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
1033774958
Device Listing 1033774958
Listing Summary
#
Listing key
1033774958
Premarket submission
K133967
Device
INTERBODY CAGE SYSTEM
Applicant
Aurora Spine
Product code
MAX
Decision date
2014-01-31
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
164775
3010326971
3010326971
AURORA SPINE, INC.
1
Y
2026-01-01
1930 Palomar Point Way Suite #103 Carlsbad CA US 92008