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
1543132212
Device Listing 1543132212
Listing Summary
#
Listing key
1543132212
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
34861
2027619
2027619
EAGLE LABS, LLC
1
N
2026-01-01
815 Vikings Pkwy Ste 160 Saint Paul MN US 55121