Last synced on 14 November 2025 at 11:06 pm

Biomet Microfixation Sternal Closure System

Page Type
Cleared 510(K)
510(k) Number
K161896
510(k) Type
Special
Applicant
BIOMET MICROFIXATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/2016
Days to Decision
22 days
Submission Type
Summary

Biomet Microfixation Sternal Closure System

Page Type
Cleared 510(K)
510(k) Number
K161896
510(k) Type
Special
Applicant
BIOMET MICROFIXATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/2016
Days to Decision
22 days
Submission Type
Summary