Internal spinal fixation procedure kit, single-use - UK MHRA Medical Device Registration

Internal spinal fixation procedure kit, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 99240. 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.

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Internal spinal fixation procedure kit, single-use

MHRA Device ID: 99240•Ref: 99240

Device Type

General Medical Device

Devices

Internal spinal fixation procedure kit, single-use

Type

Class IIa

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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Internal spinal fixation procedure kit, single-use - UK MHRA Medical Device Registration

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