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
1062556968
Device Listing 1062556968
Listing Summary
#
Listing key
1062556968
Premarket submission
K153240
Device
Styrker OrthoMap Express Knee System
Applicant
Stryker Corporate
Product code
OLO
Decision date
2016-07-07
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
3779
8010177
3002821504
Kim Wiersema
1
N
2026-01-01
1941 Stryker Way Portage MI US 49002
196212
3008837339
3008837339
STRYKER EMEA Supply Chain Services
1
N
2026-01-01
Frans Maasweg 2 Venlo Limburg NL 5928 SB