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Biomet Microfixation OmniMax MMF System

Page Type
Cleared 510(K)
510(k) Number
K152326
510(k) Type
Traditional
Applicant
BIOMET MICROFIXATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2015
Days to Decision
114 days
Submission Type
Summary

Biomet Microfixation OmniMax MMF System

Page Type
Cleared 510(K)
510(k) Number
K152326
510(k) Type
Traditional
Applicant
BIOMET MICROFIXATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2015
Days to Decision
114 days
Submission Type
Summary