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
1287066243
Device Listing 1287066243
Listing Summary
#
Listing key
1287066243
Premarket submission
K102323
Device
CERVICAL STANDALONE INTERVERTEBRAL BODY FUSION DEVICE
Applicant
Theken Spine, LLC
Product code
OVE
Decision date
2010-12-16
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
188091
3012120772
3012120772
SEASPINE ORTHOPEDICS CORPORATION
1
N
2026-01-01
5770 Armada Dr Carlsbad CA US 92008