Spineguard S.A.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K241895Cannulated PsiFGuardSeptember 26, 2024
K220160PediGuard ThreadedMarch 31, 2022
K201454DSG Connect TechnologyFebruary 10, 2021
K162884SpineGuard DSG Zavation Screw SystemJanuary 12, 2017
K152747DSG Threaded Drill SystemJune 10, 2016
K143159Cannulated PediGuard Needle#1, Cannulated PediGuard Needle#2, Cannulated PediGuard Needle 120mm, CanJanuary 23, 2015
K123390PEDIGUARD NERVE DETECTOR SYSTEMAugust 8, 2013