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
1736592031
Device Listing 1736592031
Listing Summary
#
Listing key
1736592031
Premarket submission
K220610
Device
SOLO-L
Applicant
Aurora Spine, Inc.
Product code
OVD
Decision date
2022-05-27
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
164775
3010326971
3010326971
AURORA SPINE, INC.
1
Y
2026-01-01
1930 Palomar Point Way Suite #103 Carlsbad CA US 92008