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
1244784868
Device Listing 1244784868
Listing Summary
#
Listing key
1244784868
Premarket submission
K143616
Device
AccuLIF TL and PL Cage
Applicant
Stryker Corporation
Product code
MAX
Decision date
2015-03-05
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
3787
3004024955
3004024955
STRYKER SPINE
1
Y
2020-04-25
2 PEARL COURT ALLENDALE NJ US 07401