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/ Intelivation, LLC
Intelivation, 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
K231147
Hammerdesis Interphalangeal Fusion System
September 14, 2023
K212389
Advantage Lumbar System - ALIF, PLIF, DLIF, TLIF
October 29, 2021
K212185
Golden Isles Pedicle Screw System
August 19, 2021