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 - HumanTech Spine GmbH

Address:

Gewerbestrasse 5

Steinenbronn

71144

Germany

Authorised Representative/ UK Responsible Person
Name: Osteon Medical Ltd
Address:

133 Tame Road Birmingham

Birmingham

B67DG

England United Kingdom

Code/Term Type

Vertebral body prosthesis Vertebral body prosthesis Class IIb

Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Class IIb

Bone-screw internal spinal fixation system non-sterile Bone-screw internal spinal fixation system non-sterile Class IIb

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
Vertebral body prosthesis	Vertebral body prosthesis	Class IIb
Metallic spinal interbody fusion cage	Metallic spinal interbody fusion cage	Class IIb
Bone-screw internal spinal fixation system non-sterile	Bone-screw internal spinal fixation system non-sterile	Class IIb