FDA 510(k) Applications Submitted by ANKIT K SHAH
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K180851 |
04/02/2018 |
VERTEXÖ Reconstruction System |
Medtronic Sofamor Danek USA, Inc |
K132700 |
08/29/2013 |
PERIMETER INTERBODY FUSION DEVICE |
MEDTRONIC SOFAMOR DANEK, INC. |
K133216 |
10/18/2013 |
CRESCENT SPINAL SYSTEM |
MEDTRONIC SOFAMOR DANEK, INC. |
K160418 |
02/16/2016 |
PERIMETER Interbody Fusion Device |
Medtronic Sofamor Danek USA, Inc |
K171031 |
04/06/2017 |
CRESCENTÖ Spinal System |
Medtronic Sofamor Danek |
K161210 |
04/28/2016 |
RIALTO(TM) SI Fusion System, Medtronic Reusable Instruments for Use with the IPC(TM) Powerease(TM) System, and Medtronic Navigated Manual Reusable Instruments for use with the StealthStation(TM) and IPC(TM) Powerease(TM) Systems |
Medtronic Sofamor Danek |
K171468 |
05/18/2017 |
FUSE Spinal System |
Medtronic Sofamor Danek |
K182119 |
08/06/2018 |
CD HORIZONÖ Spinal System |
Medtronic Sofamor Danek USA, Inc. |
K182436 |
09/07/2018 |
POWEREASE System |
Medtronic Sofamor Danek USA, Inc. |
K173249 |
10/10/2017 |
CD HORIZONÖ Spinal System |
Medtronic Sofamor Danek USA, Inc. |
K183197 |
11/19/2018 |
PYRAMESHÖ Implant System |
Medtronic Sofamor Danek USA, INC. |
K153589 |
12/16/2015 |
CD HORIZON Spinal System |
MEDTRONIC SOFAMOR DANEK USA, INC. |
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