Last synced on 30 May 2025 at 11:05 pm

BRM TOOL Screws, BIOPLAN Subtalar Implant

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222820
510(k) Type
Traditional
Applicant
BRM Extremities
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
12/16/2022
Days to Decision
88 days
Submission Type
Summary

BRM TOOL Screws, BIOPLAN Subtalar Implant

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222820
510(k) Type
Traditional
Applicant
BRM Extremities
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
12/16/2022
Days to Decision
88 days
Submission Type
Summary