Medical Device Manufacturer · US , Monterey , CA

Elevation Spine

2 submissions · 2 cleared · Since 2019
2
Total
2
Cleared
0
Denied

Elevation Spine — FDA 510(k) Submissions

Elevation Spine has submitted 2 FDA 510(k) premarket notifications since 2019, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Intervertebral Fusion Device With Integrated Fixation, Cervical . Use the specialty filter in the sidebar to narrow results.

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