Episealer Patellofemoral System
Dec 2022
259d
Episurf Medical, Inc.
1
Total
1
Cleared
0
Denied
Episurf Medical, Inc. — FDA 510(k) Submissions
Episurf Medical, Inc. 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 Prosthesis, Knee, Patello/femoral, Semi-constrained, Cemented, Metal/polymer . Use the specialty filter in the sidebar to narrow results.
1 devices