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
1467044876
Device Listing 1467044876
Listing Summary
#
Listing key
1467044876
Premarket submission
K132505
Device
ACCULIF TL AND PL CAGE
Applicant
Coalign Innovations, Inc.
Product code
MAX
Decision date
2013-09-12
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
339166
3004024955
3004024955
STRYKER SPINE
1
N
2026-01-01
2 PEARL COURT ALLENDALE NJ US 07401