Kiscomedica S.A.

FDA Regulatory Profile

Summary

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

Recent Recalls

NumberClassProductDate
Z-1461-2017Class IIL-Varlock Cage/Trial Implant Holder, Reference HD0060, Kisco International, France. Product UsageJanuary 11, 2017

Recent 510(k) Clearances

K-NumberDeviceDate
K080537L-VARLOCKJune 30, 2008