Medical Device Manufacturer · US , Boca Raton , FL

Bright Spine

2 submissions · 2 cleared · Since 2020
2
Total
2
Cleared
0
Denied

Bright Spine — FDA 510(k) Submissions

Bright Spine has submitted 2 FDA 510(k) premarket notifications since 2020, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Spinal Vertebral Body Replacement Device - Cervical . Use the specialty filter in the sidebar to narrow results.

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