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
1351739311
Device Listing 1351739311
Listing Summary
#
Listing key
1351739311
Premarket submission
K180822
Device
VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion System
Applicant
Wenzel Spine, Inc.
Product code
MAX
Decision date
2019-01-28
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
283021
3006172536
3006172536
Wenzel Spine
1
N
2026-01-01
2535 Brockton Dr Ste 450 Austin TX US 78758