Medical Device Manufacturer · US , Walnut Creek , CA

Acorn Group, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1990
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Acorn Group, Inc. Orthopedic ✕
1 devices
1-1 of 1
Cleared Apr 29, 1992
TOP CERVICAL SPINE PLATES & TITANIUM BONE SCREWS
K914362 · KWQ
Orthopedic · 211d
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All4 General & Plastic Surgery 2 Orthopedic 1 Anesthesiology 1