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
1475000218
Device Listing 1475000218
Listing Summary
#
Listing key
1475000218
Premarket submission
K113789
Device
MODULAR PROXIMALLY FLUTED HIP STEM
Applicant
Smith & Nephew, Inc.
Product code
MEH
Decision date
2012-04-19
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
117364
1225675
3001451451
Tecomet Inc.
1
N
2026-01-01
115 Eames Street Wilmington MA US 01887