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
1330638394
Device Listing 1330638394
Listing Summary
#
Listing key
1330638394
Premarket submission
K161173
Device
Avenue® T TLIF Cage
Applicant
Ldr Spine USA, Inc.
Product code
OVD
Decision date
2016-09-28
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
162534
3010462278
3010462278
SIMAGEC
1
N
2026-01-01
54 avenue de la Plaine Z.I. ROUSSET CEDEX Bouches-du-Rhone FR 13106