Osteotech, Inc. - FDA 510(k) Cleared Devices
Recent clearances: GRAFTON R II EDBM, DEMINERALIZED BONE MATRIX ALLOGRAFT, RESORBABLE CALCIUM SALT BONE VOID FILLER DEVICES, PLEXUR M, PLEXUR-P
24
Total
21
Cleared
0
Denied
FDA 510(k) Regulatory Record - Osteotech, Inc. Pathology ✕
1 devices