Wrightmedicaltechnologyinc - FDA 510(k) Cleared Devices
Recent clearances: Prophecy Preoperative Navigation Alignment System, PRO-DENSE LoVisc Bone Graft Substitute, Sterile PHALINX Hammertoe System
302
Total
291
Cleared
0
Denied
FDA 510(k) Regulatory Record - Wrightmedicaltechnologyinc Ear, Nose, Throat ✕
1 devices