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510(k) K152326

Biomet Microfixation OmniMax MMF System by Biomet Microfixation — Product Code JEY

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 10, 2015
Date Received
August 18, 2015
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Plate, Bone
Device Class
Class II
Regulation Number
872.4760
Review Panel
DE
Submission Type

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