Covidien (Part of Medtronic) - FDA 510(k) Cleared Devices
Recent clearances: Tri-staple 2.0™ Reloads, Signia™ Circular Adapter (Standard Length) (SIGCIRSTND)
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Covidien (Part of Medtronic) General & Plastic Surgery ✕
2 devices