Ortho Development Corp. - FDA 510(k) Cleared Devices
Recent clearances: Balanced Knee System TriMax Porous Femoral Components, Trivicta® Hip Stem, BKS Revision System
45
Total
43
Cleared
0
Denied
FDA 510(k) Regulatory Record - Ortho Development Corp. Gastroenterology & Urology ✕
1 devices