Bioplate, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MODIFIED STERILE PLATE & SCREW KIT CONFIGURATIONS FOR USE WITH BIOPLATE TITANIUM FIXATION SYSTEM, MOFICATION TO: MODIFIED PLATE DESIGN FOR BIOPLATE ZIP CRANIOTOMY FIXATION, MODIFIED PLATE DESIGN FOR BIOPLATE ZIP CRANIOTOMY FIXATION SYSTEM
23
Total
23
Cleared
0
Denied
FDA 510(k) Regulatory Record - Bioplate, Inc. Orthopedic ✕
1 devices