21 CFR Chapter I Subchapter H โ Medical Devices โ Part 890 Physical Medicine Devices From Food and Drug Administration (FDA) ๐บ๐ธ Regulation on physical medicine devices under 21 CFR Chapter I Subchapter H - Medical Devices - Part 890. Metadata quality: Metadata quality: Data description filled Files documented License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 77.77777777777779/100 Updated 2 weeks ago Other (Public Domain) 0 reuses 0 favorites
21 CFR Chapter I Subchapter H โ Medical Devices โ Part 888 Orthopedic Devices From Food and Drug Administration (FDA) ๐บ๐ธ This document is a regulation titled "21 CFR Chapter I Subchapter H โ Medical Devices โ Part 888 Orthopedic Devices". Metadata quality: Metadata quality: Data description filled Files documented License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 77.77777777777779/100 Updated 2 weeks ago Other (Public Domain) 0 reuses 0 favorites
Defining joint replacement medical devices and ancillary medical devices From Therapeutic Goods Administration (TGA) ๐ฆ๐บ Guidance for manufacturers and sponsors on shoulder, hip and knee joint replacement medical devices and ancillary medical devices. Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on March 27, 2024 Other (Non-Commercial) 0 reuses 0 favorites
Guidance Document For The Preparation of Premarket Notification For Ceramic Ball Hip Systems From Food and Drug Administration (FDA) ๐บ๐ธ A guidance document for preparing premarket notifications for ceramic ball hip systems. Focuses on premarket requirements. Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are closed Temporal coverage filled Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on March 17, 2020 Other (Public Domain) 0 reuses 0 favorites
Metal-on-metal hip replacement implants From Therapeutic Goods Administration (TGA) ๐ฆ๐บ Overseas advice for general practitioners, orthopaedic surgeons and other health professionals on metal-on-metal hip replacement implants. Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on July 14, 2017 Other (Non-Commercial) 0 reuses 0 favorites
Metal-on-metal hip implants: Information for patients From Therapeutic Goods Administration (TGA) ๐ฆ๐บ Advice for patients on metal-on-metal hip replacement implants. Metadata quality: Metadata quality: Data description empty Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 55.55555555555556/100 Updated on July 14, 2017 Other (Non-Commercial) 0 reuses 0 favorites
Effective Date of Requirement for Premarket Approval for Total Metal-on-Metal Semi-Constrained Hip Joint Systems From Food and Drug Administration (FDA) ๐บ๐ธ Document number 2016-03331. The Food and Drug Administration (FDA) is issuing a final order to require the filing of a premarket approval application (PMA) or a notice of completion of a product development protocol (PDP) for the hip joint metal/metal semi-constrained, with a cemented acetabularโฆ Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on February 18, 2016 Other (Public Domain) 0 reuses 0 favorites
Safety of Metal-on-Metal joint replacements with a particular focus on hip implants From European Commission ๐ช๐บ Safety of Metal-on-Metal joint replacements with a particular focus on hip implants Metadata quality: Metadata quality: Data description empty Files documentation missing License filled Update frequency not followed File formats are closed Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 44.44444444444444/100 Updated on December 1, 2021 Creative Commons Attribution 4.0 0 reuses 0 favorites
Effective Date of Requirement for Premarket Approval for Two Class III Preamendments Devices From Food and Drug Administration (FDA) ๐บ๐ธ Document number 2013-01006. The Food and Drug Administration (FDA) is proposing to require the filing of a premarket approval application (PMA) or a notice of completion of a product development protocol (PDP) for the following two class III preamendments devices: Hip joint metal/metal semi-โฆ Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on January 18, 2013 Other (Public Domain) 0 reuses 0 favorites
On the accreditation of Sichuan Medical Devices Biomaterials and Products Inspection Center for hip prosthesis and other medical devices and project testing qualifications notice From National Medical Products Administration (NMPA) ๐จ๐ณ FGWJ-2012-10072 Metadata quality: Metadata quality: Data description empty Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 55.55555555555556/100 Updated on February 29, 2012 Other (Public Domain) 0 reuses 0 favorites
Provision No. 539/12 From National Administration of Drugs, Food and Medical Devices (ANMAT) ๐ฆ๐ท The "Official List of Implants Released for Commercialization and Use" (LOI) is created. The list shall cover the following products: breast implants, hip prostheses, knee prostheses and spine implants. B.O. January 31, 2012. Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are closed Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 55.55555555555556/100 Updated on January 1, 2012 Creative Commons Attribution 4.0 0 reuses 0 favorites
Commission Directive 2005/50/EC of 11 August 2005 on the reclassification of hip, knee and shoulder joint replacements in the framework of Council Directive 93/42/EEC concerning medical devices (Text with EEA relevance) From European Parliament ๐ช๐บ Commission Directive 2005/50/EC reclassifies hip, knee, and shoulder joint replacements under Council Directive 93/42/EEC on medical devices. Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on August 11, 2005 Creative Commons Attribution 4.0 0 reuses 0 favorites
On the accreditation of Tianjin Medical Devices Quality Supervision and Inspection Center on hip prosthesis and other products and projects testing notice From National Medical Products Administration (NMPA) ๐จ๐ณ FGWJ-2005-10218 Metadata quality: Metadata quality: Data description empty Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 55.55555555555556/100 Updated on March 10, 2024 Other (Public Domain) 0 reuses 0 favorites
Notice on the Investigation and Handling of Unqualified and Unlicensed Artificial Hip (Knee) Joint Products From National Medical Products Administration (NMPA) ๐จ๐ณ FGWJ-2002-10334 Metadata quality: Metadata quality: Data description empty Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 55.55555555555556/100 Updated on March 10, 2024 Other (Public Domain) 0 reuses 0 favorites
S.I. No. 92/2007 - European Communities (Medical Devices) (Reclassification of Hip, Knee and Shoulder Joint Replacements) (Amendment) Regulations 2007 From Health Products Regulatory Authority (HPRA) ๐ฎ๐ช A statutory instrument from 2007 amending regulations related to the reclassification of hip, knee, and shoulder joint replacements in the European Communities. Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on May 8, 2024 Other (Public Domain) 0 reuses 0 favorites