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

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Manufacturer's Devices - Woven Orthopedic Technologies LLC

Address:

63 East Center Street Manchester

Hartford

CT 06040

United States

Authorised Representative/ UK Responsible Person
Name: Ortho Consulting Group Ltd
Address:

Building 81 Greenham Business Park

Newbury

Berkshire RG19 6HW

England United Kingdom

Code/Term Type

Trans-facet-screw internal spinal fixation system sterile Trans-facet-screw internal spinal fixation system sterile Class IIb

Contact details

Freedom of information

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

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