Medical Device Manufacturer · US , Andover , MA

Smith & Nephew Dyonics, Inc. - FDA 510(k) Cleared Devices

22 submissions · 19 cleared · Since 1990
22
Total
19
Cleared
0
Denied
FDA 510(k) Regulatory Record - Smith & Nephew Dyonics, Inc. Orthopedic
16 devices
1-16 of 16
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