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
1050060098
Device Listing 1050060098
Listing Summary
#
Listing key
1050060098
Premarket submission
K994286
Device
ZMR HIP SYSTEM-POROUS REVISION
Applicant
Zimmer, Inc.
Product code
LPH
Decision date
2000-03-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
3870
1822565
1000220733
ZIMMER, INC.
1
Y
2026-01-01
1800 W. Center Street WARSAW IN US 46580