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
1467366738
Device Listing 1467366738
Listing Summary
#
Listing key
1467366738
Premarket submission
K151198
Device
A-CIFT SoloFuse
Applicant
Spinefrontier, Inc.
Product code
OVE
Decision date
2015-07-17
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
25573
3005977257
3005977257
SPINEFRONTIER, INC. DBA LESspine Innovations
1
N
2026-01-01
200 Summit Drive Suite 505 Burlington MA US 01803