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/ Kalitec Medical, LLC
Kalitec Medical, LLC
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K230974
NIDO Pedicle Screw System
September 15, 2023
K220902
Navagio Lumbar Cage
May 27, 2022
K182210
TiWAVE-L Porous Titanium Lumbar Cage
January 7, 2019