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Brm Extremities Srl

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K220142BRM Digitalis SpacerApril 4, 2023
K222820BRM TOOL Screws, BIOPLAN Subtalar ImplantDecember 16, 2022
K203773BRM TOOL ScrewsJanuary 14, 2022
K191966NewPrim SystemFebruary 13, 2020