Anulex Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MICRO/MINI N-PK(F) BONE ANCHOR, MICRO/MINI N-PK(H) BONE ANCHOR, FIXATE TISSUE BAND
12
Total
12
Cleared
0
Denied
FDA 510(k) Regulatory Record - Anulex Technologies, Inc. Orthopedic ✕
3 devices