FDA 510(k) Applications Submitted by STEPHANE BETTE
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K220160 |
01/19/2022 |
PediGuard Threaded |
Spine Guard S.A. |
| K201454 |
06/01/2020 |
DSG Connect Technology |
SpineGuard, S.A. |
| K152747 |
09/23/2015 |
DSG Threaded Drill System |
SPINEGUARD, S.A. |
| K162884 |
10/14/2016 |
SpineGuard DSG Zavation Screw System |
SPINEGUARD,S.A. |
| K143159 |
11/03/2014 |
Cannulated PediGuard Needle#1, Cannulated PediGuard Needle#2, Cannulated PediGuard Needle 120mm, Cannulated PediGuard Handle; PediGuard Tri Tip ╪4.0mm, PediGuard Tri Tip ╪3.2mm, PediGuard Tri Tip ╪2.5mm, PediGuard ╪2.5mm XS, PediGuard Curv, PediGuard Curv |
SpineGuard, S.A. |
|
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