Smith & Nephew Inc., Endoscopy Div. - FDA 510(k) Cleared Devices
Recent clearances: REGENETEN™ Bioinductive Implant, ACUFEX DIRECTOR APPLICATION ANATOMIC GUIDE SYSTEM, SMITH & NEPHEW HIP ARTHROSCOPY REPAIR INSTRUMENT TRAY
10
Total
10
Cleared
0
Denied
FDA 510(k) Regulatory Record - Smith & Nephew Inc., Endoscopy Div. General Hospital ✕
3 devices