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
1489417467
Device Listing 1489417467
Listing Summary
#
Listing key
1489417467
Premarket submission
K971854
Device
OSTEOLOCK ACETABULAR SHELL SYSTEM
Applicant
Howmedica Corp.
Product code
LPH
Decision date
1997-07-30
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
3773
2249697
3003070421
HOWMEDICA OSTEONICS CORP
1
Y
2026-01-01
325 CORPORATE DR. MAHWAH NJ US 07430