Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1320274978
Device Listing 1320274978
Listing Summary
#
Listing key
1320274978
Premarket submission
K152326
Device
Biomet Microfixation OmniMax MMF System
Applicant
Biomet Microfixation
Product code
JEY
Decision date
2015-12-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
28267
1032347
1032347
BIOMET MICROFIXATION
1
N
2026-01-01
1520 Tradeport Dr Jacksonville FL US 32218