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
1244654528
Device Listing 1244654528
Listing Summary
#
Listing key
1244654528
Premarket submission
K133366
Device
ORTHROS POSTERIOR STABILIZATION SYSTEM
Applicant
Camber Spine
Product code
NKB
Decision date
2014-04-08
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
157238
3010197239
3010197239
CAMBER SPINE TECHNOLOGIES
1
N
2026-01-01
501 Allendale Rd King of Prussia PA US 19406