Last synced on 14 November 2025 at 11:06 pm

Pectus Support Bar System

Page Type
Cleared 510(K)
510(k) Number
K213712
510(k) Type
Traditional
Applicant
Biomet Microfixation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/2022
Days to Decision
107 days
Submission Type
Summary

Pectus Support Bar System

Page Type
Cleared 510(K)
510(k) Number
K213712
510(k) Type
Traditional
Applicant
Biomet Microfixation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/2022
Days to Decision
107 days
Submission Type
Summary