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
1149302519
Device Listing 1149302519
Listing Summary
#
Listing key
1149302519
Premarket submission
K163481
Device
HALF DOME Posterior Lumbar Interbody System
Applicant
Astura Medical
Product code
MAX
Decision date
2017-05-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
235708
3015941638
3011764740
Astura Medical
1
N
2026-01-01
4949 W Royal Ln Irving TX US 75063