Medical Device Manufacturer · US , Menlo Park , CA

Intersect Ent.

1 submissions · 1 cleared · Since 2022
1
Total
1
Cleared
0
Denied

Intersect Ent. — FDA 510(k) Submissions

Intersect Ent. has submitted 1 FDA 510(k) premarket notifications since 2022, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Instrument, Ent Manual Surgical . Use the specialty filter in the sidebar to narrow results.

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