Company ยท FR
Spineguard S.A.
FDA 510(k) clearances and medical device recalls filed under this name, 2013 to 2024. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 26, 2024 | K241895 | Cannulated PsiFGuard Spineguard, FR | SCY |
| Mar 31, 2022 | K220160 | PediGuard Threaded Spineguard S.A., FR | PDQ |
| Feb 10, 2021 | K201454 | DSG Connect Technology Spineguard S.A., FR | PDQ |
| Jan 12, 2017 | K162884 | SpineGuard DSG Zavation Screw System Spineguard S.A., FR | HBG |
| Jun 10, 2016 | K152747 | DSG Threaded Drill System Spineguard S.A., FR | PDQ |
| Jan 23, 2015 | K143159 | Cannulated PediGuard Needle#1, Cannulated PediGuard Needle#2, Cannulated PediGuard Needle 120mm, Cannulated PediGuard Ha Spineguard S.A., FR | PDQ |
| Aug 8, 2013 | K123390 | PEDIGUARD NERVE DETECTOR SYSTEM Spineguard S.A. | PDQ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||