FDA 510(k) Applications Submitted by SpineGuard, S.A.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K123390 |
11/02/2012 |
PEDIGUARD NERVE DETECTOR SYSTEM |
SPINEGUARD, S.A. |
K201454 |
06/01/2020 |
DSG Connect Technology |
SpineGuard, S.A. |
K152747 |
09/23/2015 |
DSG Threaded Drill 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. |
|
|