Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

Back to MHRA

Manufacturer's Devices - Cartiva Inc.

Address:

6120 Windward Parkway Suite 220

Alpharetta

Georgia 30005

United States

Authorised Representative/ UK Responsible Person
Name: Stryker UK Ltd
Address:

Stryker House Hambridge Road

Newbury

Berkshire RG14 5AW

England United Kingdom

Code/Term Type

Orthopaedic prosthesis implantation positioning instrument single-use Orthopaedic prosthesis implantation positioning instrument single-use Class IIa

Partial metatarsophalangeal joint prosthesis Partial metatarsophalangeal joint prosthesis Class IIb

Surgical drill guide reusable Surgical drill guide reusable Class IIb

Orthopaedic prosthesis implantation positioning instrument reusable Orthopaedic prosthesis implantation positioning instrument reusable Class I

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

© 2011 Crown Copyright. To contact us about this website, use our feedback form.

Code/Term		Type
Orthopaedic prosthesis implantation positioning instrument single-use	Orthopaedic prosthesis implantation positioning instrument single-use	Class IIa
Partial metatarsophalangeal joint prosthesis	Partial metatarsophalangeal joint prosthesis	Class IIb
Surgical drill guide reusable	Surgical drill guide reusable	Class IIb
Orthopaedic prosthesis implantation positioning instrument reusable	Orthopaedic prosthesis implantation positioning instrument reusable	Class I