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
1336739445
Device Listing 1336739445
Listing Summary
#
Listing key
1336739445
Premarket submission
K970194
Device
PROFORM CEMENTED TITANIUM REVISION FEMORAL COMPONENT
Applicant
Stelkast Company
Product code
JDI
Decision date
1997-04-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
47081
2530191
1000307053
STELKAST COMPANY
1
N
2020-04-25
200 HIDDEN VALLEY RD. Canonsburg PA US 15317