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Biomet Microfixation OmniMax MMF System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202969
510(k) Type
Traditional
Applicant
Biomet Microfixation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2021
Days to Decision
309 days
Submission Type
Summary

Biomet Microfixation OmniMax MMF System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202969
510(k) Type
Traditional
Applicant
Biomet Microfixation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2021
Days to Decision
309 days
Submission Type
Summary