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
1430246494
Device Listing 1430246494
Listing Summary
#
Listing key
1430246494
Premarket submission
K180071
Device
STYLO Interbody Fusion Device
Applicant
Legend Spine Technologies
Product code
MAX
Decision date
2018-05-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
222930
3015176639
3015176639
LEGEND SPINE
1
N
2020-04-25
346 Barnsbury Rd Langhorne PA US 19047