Partial-resurfacing knee femur prosthesis - UK MHRA Medical Device Registration

Partial-resurfacing knee femur prosthesis is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 184352. The device is manufactured by Cartiva, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Stryker UK Ltd.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Partial-resurfacing knee femur prosthesis

MHRA Device ID: 184352•Ref: 184352

Device Type

General Medical Device

Devices

Partial-resurfacing knee femur prosthesis

Type

Class IIb

Date Registered

Jun 3, 2024

Last Updated

Feb 1, 2024

Manufacturer Information

Name

Cartiva, Inc.

Address

6120 Windward Parkway Suite 220

Alpharetta, Georgia, United States

Created Date

Apr 30, 2021

Authorized Representative

Name

Stryker UK Ltd

Relationship Type

UK Responsible Person

Address

Stryker House Hambridge Road

Newbury, Berkshire, England, United Kingdom

Postcode: RG14 5AW

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Partial-resurfacing knee femur prosthesis - UK MHRA Medical Device Registration

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