Medtronic Sofamor Danek USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Catalyft PL Expandable Interbody System, Symmetrix™ L Spinal System, OsteoCool™ RF Ablation System
173
Total
162
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medtronic Sofamor Danek USA, Inc. General Hospital ✕
4 devices
Cleared
Oct 15, 2019
Medtronic Transportation / Sterilization Cassettes
General Hospital
197d
Cleared
Feb 23, 2017
Medtronic Transportation/Sterilization Cassettes
General Hospital
94d
Cleared
Jan 20, 2016
Medtronic Transportation/Sterilization Cassettes
General Hospital
163d
Cleared
Dec 08, 2006
MEDTRONIC GRAFT DELIVERY SYRINGE
General Hospital
70d