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
1358913904
Device Listing 1358913904
Listing Summary
#
Listing key
1358913904
Premarket submission
K133717
Device
LONGBOW SPACER SYSTEM
Applicant
Life Spine
Product code
MAX
Decision date
2014-09-19
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
99255
3007406875
3007406875
GIZMO PRECISION MEDICAL LLC
1
Y
2020-04-25
6N343 Mission Hills Drive St Charles IL US 60175