Spineguard S.A.

FDA Regulatory Profile

Spineguard S.A. appears in FDA public data with 0 recalls, 7 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 26, 2024.

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