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
1520775765
Device Listing 1520775765
Listing Summary
#
Listing key
1520775765
Premarket submission
K131296
Device
VARILIFT-L INTERBODY FUSION DEVICE
Applicant
Wenzel Spine, Inc.
Product code
MAX
Decision date
2013-09-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
110024
3008009850
3008009850
WENZEL SPINE, Inc.
1
N
2020-04-25
1130 Rutherford Lane Suite 200 Austin TX US 78753