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
1296300652
Device Listing 1296300652
Listing Summary
#
Listing key
1296300652
Premarket submission
K002960
Device
TRILOGY ACETABULAR SYSTEM LARGE HEAD LINER, MODEL 6353
Applicant
Zimmer, Inc.
Product code
LPH
Decision date
2000-12-11
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
3870
1822565
1000220733
ZIMMER, INC.
1
Y
2027-01-01
1800 W. Center Street WARSAW IN US 46580
3882
2648920
1000132037
ZIMMER MANUFACTURING B.V.
1
N
2027-01-01
ROUTE 1, KM. 123.4, BLDG. 2 TURPEAUX INDUSTRIAL PARK MERCEDITA PR US 00715