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
1195025387
Device Listing 1195025387
Listing Summary
#
Listing key
1195025387
Premarket submission
K121342
Device
XIA 4.5 SPINAL SYSTEM
Applicant
Stryker Corp.
Product code
NKB
Decision date
2012-06-22
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