Bone-screw internal spinal fixation system connector - UK MHRA Medical Device Registration
Bone-screw internal spinal fixation system connector is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 205921. The device is manufactured by K2M Group Holdings, Inc from United States, classified as General Medical Device.
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Device Type
General Medical Device
Type
Class IIb
Status
Date Registered
Nov 28, 2024
Address
600 Hope Parkway SE
Leesburg, Virginia, United States
External orthopaedic fixation system, reusable
Type: General Medical Device
Manufacturer: Orthofix S.r.l.
External orthopaedic fixation system, single-use
Type: General Medical Device
Manufacturer: Orthofix S.r.l.
Bone nail guidewire, reusable
Type: General Medical Device
Manufacturer: Orthofix S.r.l.
External orthopaedic fixation frame calculation software
Type: General Medical Device
Manufacturer: Orthofix S.r.l.
External orthopaedic fixation system, reusable
Type: General Medical Device
Manufacturer: Orthofix S.r.l.
External orthopaedic fixation system, single-use
Type: General Medical Device
Manufacturer: Orthofix S.r.l.
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Manufacturer: Orthofix S.r.l.
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Manufacturer: Orthofix S.r.l.
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Manufacturer: Orthofix S.r.l.
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Type: General Medical Device
Registered: Nov 28, 2024
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Type: General Medical Device
Registered: Nov 28, 2024
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Registered: Nov 28, 2024
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Registered: Nov 28, 2024