Arthrotek/Biomet, Inc. - FDA 510(k) Cleared Devices
Recent clearances: WASHERLOC SCREW SYSTEM, LIGAMENT SCREW SYSTEM, NO-PROFILE BI-CORTICAL SCREW SYSTEM, CHANNEL LIGAMENT CLAMP, HECKMAN SCRE
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Arthrotek/Biomet, Inc. Orthopedic ✕
1 devices