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
1969818539
Device Listing 1969818539
Listing Summary
#
Listing key
1969818539
Premarket submission
K141850
Device
FLOSPINE PEDICLE SCREW SYSTEM
Applicant
Flospine
Product code
NKB
Decision date
2014-10-27
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
180691
3011513267
3011513267
FLOSPINE LLC
1
N
2026-01-01
3998 FAU Blvd Suite 300 Boca Raton FL US 33431