Medical Device Manufacturer · US , Cambridge , MA

Zsfab, Inc.

4 submissions · 4 cleared · Since 2021
4
Total
4
Cleared
0
Denied

Zsfab, Inc. — FDA 510(k) Submissions

Zsfab, Inc. has submitted 4 FDA 510(k) premarket notifications since 2021, of which 4 received clearance as substantially equivalent to a predicate device.

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

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