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
1022431651
Device Listing 1022431651
Listing Summary
#
Listing key
1022431651
Premarket submission
K110906
Device
APEX SPINE SYSTEM
Applicant
Spinecraft, LLC
Product code
NKB
Decision date
2011-07-26
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
63887
3004717358
3004717358
SPINECRAFT LLC
1
N
2026-01-01
777 Oakmont Ln Suite 200 Westmont IL US 60559