Brm Extremities

FDA Regulatory Profile

Brm Extremities appears in FDA public data with 0 recalls, 4 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 4, 2023.

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