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
1289356737
Device Listing 1289356737
Listing Summary
#
Listing key
1289356737
Premarket submission
K142251
Device
AVS AS PEEK Spacer
Applicant
Stryker Corporation
Product code
ODP
Decision date
2014-11-19
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
3765
9617544
3003112432
Oonagh Lahiff
1
N
2020-04-25
2 Pearl Court Allendale NJ US 07401
3787
3004024955
3004024955
STRYKER SPINE
1
Y
2020-04-25
2 PEARL COURT ALLENDALE NJ US 07401