Spinal guidewire - UK MHRA Medical Device Registration

Spinal guidewire is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 205916. The device is manufactured by K2M Group Holdings, Inc from United States, classified as General Medical Device.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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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MHRA Registered

General Medical Device

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Spinal guidewire

MHRA Device ID: 205916

Device Type

General Medical Device

Type

Class IIa

Status

DREGIY

Date Registered

Dec 21, 2024

Manufacturer Information

Name

K2M Group Holdings, Inc

Address

600 Hope Parkway SE

Leesburg, Virginia, United States

DJ Fang

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Other Products from K2M Group Holdings, Inc (10)

Spinal guidewire - UK MHRA Medical Device Registration

Device Type

Type

Status

Date Registered

Name

Address

DJ Fang

Fluted surgical drill bit, single-use

General internal orthopaedic fixation system implantation kit

External orthopaedic fixation system, single-use

Fluted surgical drill bit, reusable

Fluted surgical drill bit, single-use

General internal orthopaedic fixation system implantation kit

External orthopaedic fixation system, reusable

External orthopaedic fixation system, single-use

External orthopaedic fixation system, single-use

General internal orthopaedic fixation system implantation kit

Spinal guidewire

Scalpel, single-use

Surgical torque wrench, reusable

Spinal implant trial

Orthopaedic bone screw starter/notcher

Bone-screw internal spinal fixation system connector

Surgical instrument handle, torque-limiting

Surgical torque wrench, reusable

Spinal bone screw, non-bioabsorbable

Orthopaedic instrument extractor