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
1852223116
Device Listing 1852223116
Listing Summary
#
Listing key
1852223116
Premarket submission
P010014
Device
OXFORD(TM) MENISCAL UNICOMPARTMENTAL KNEE SYSTEM
Applicant
BIOMET MANUFACTURING CORP.
Product code
NRA
Decision date
2004-04-21
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
195477
3013055499
3013055499
Stephanie Lynch
1
N
2026-01-01
1800 W Center St Warsaw IN US 46580