510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K202969Substantially Equivalent

Biomet Microfixation OmniMax MMF System

Biomet Microfixation, Jacksonville FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K202969 is the FDA 510(k) clearance record for Biomet Microfixation OmniMax MMF System, a class II device, cleared for Biomet Microfixation on under FDA product code JEY (Plate, Bone). FDA records list 86 510(k) clearances for Biomet Microfixation, from to . As of , FDA records show no recalls naming K202969.

Clearance record

Decision date
Received
(309 days to decision)
Product code
JEY Plate, Bone
Regulation
21 CFR 872.4760
Device class
Class II
Review panel
Dental
Applicant
Biomet Microfixation 1520 Tradeport Dr., Jacksonville FL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JEY

Trailing 12 months
5 clearances under product code JEY in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JEY, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20261
August 20261
September 20260
October 20260