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 - Spinal Kinetics LLC

Address:

501 Mercury Drive

Sunnyvale

94085

United States

Authorised Representative/ UK Responsible Person
Name: Emergo Consulting (UK) Limited
Address:

Compass House Vision Park Histon c/o Cr360 – UL International

Cambridge

CB24 9BZ

England United Kingdom

Code/Term Type

Cervical total intervertebral disc prosthesis modular Cervical total intervertebral disc prosthesis modular Class IIb

Orthopaedic surgical procedure kit non-medicated reusable Orthopaedic surgical procedure kit non-medicated reusable Class I

Lumbar total intervertebral disc prosthesis Lumbar total intervertebral disc prosthesis 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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Code/Term		Type
Cervical total intervertebral disc prosthesis modular	Cervical total intervertebral disc prosthesis modular	Class IIb
Orthopaedic surgical procedure kit non-medicated reusable	Orthopaedic surgical procedure kit non-medicated reusable	Class I
Lumbar total intervertebral disc prosthesis	Lumbar total intervertebral disc prosthesis	Class IIb