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
1957542842
Device Listing 1957542842
Listing Summary
#
Listing key
1957542842
Premarket submission
K130412
Device
OSTEOMED EXTREMIFUSE SYSTEM
Applicant
Osteomed
Product code
HWC
Decision date
2013-05-31
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
42486
2027754
2027754
OSTEOMED
1
Y
2026-01-01
3885 Arapaho Rd ADDISON TX US 75001