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
1379367802
Device Listing 1379367802
Listing Summary
#
Listing key
1379367802
Premarket submission
K122798
Device
INTEGRIP ACETABULAR SHELL, INTEGRIP REVISION ACETABULAR SHELL
Applicant
Exactech, Inc.
Product code
LPH
Decision date
2012-10-11
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
28815
1038671
1038671
EXACTECH, INC.
1
Y
2026-01-01
2320 N.W. 66TH CT. GAINESVILLE FL US 32653