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
1811771823
Device Listing 1811771823
Listing Summary
#
Listing key
1811771823
Premarket submission
K162694
Device
Ayers Rock Cervical interbody fusion system
Applicant
Spineway
Product code
ODP
Decision date
2017-01-12
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
163409
1000461041
1000461041
Stephan TOUPIN
1
N
2026-01-01
7320 NW, 12th street suite 103 Miami FL US 33126