Conmed Linvatec - FDA 510(k) Cleared Devices
Recent clearances: Y-KNOT ALL-SUTURE ANCHOR MODEL HF13, MATRYX INTERFERENCE SCREW (5.0-6.5MM), CONMED LINVATEC SEQUENT MENISCAL REPAIR DEVICE
21
Total
21
Cleared
0
Denied
FDA 510(k) Regulatory Record - Conmed Linvatec Neurology ✕
1 devices