Bone-screw internal spinal fixation system, sterile - UK MHRA Medical Device Registration

Bone-screw internal spinal fixation system, sterile is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 69768. The device is manufactured by K2M Group Holdings, 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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Bone-screw internal spinal fixation system, sterile

MHRA Device ID: 69768•Ref: 69768

Device Type

General Medical Device

Devices

Bone-screw internal spinal fixation system, sterile

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Jan 30, 2024

Manufacturer Information

Name

K2M Group Holdings, Inc

Address

600 Hope Parkway SE

Leesburg, Virginia, United States

Created Date

Mar 17, 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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Bone-screw internal spinal fixation system, sterile - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

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