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Biomet Micofixation

FDA Regulatory Profile

Biomet Micofixation appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 23, 2022.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K2130722.1 x 255mm Drill, 22mm StopAugust 23, 2022
K212841Pectus Blu Support Bar SystemJanuary 7, 2022
K203474Biomet Microfixation RibFix Advantage SystemJanuary 28, 2021

FDA data resources