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
1274313819
Device Listing 1274313819
Listing Summary
#
Listing key
1274313819
Premarket submission
K131540
Device
INTERFUSE L INTERVERTEBRAL BODY FUSION DEVICE
Applicant
Vertebral Technologies, 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
151957
3010020754
3010020754
NEXT ORTHOSURGICAL
1
N
2020-04-25
3270 Corporate Vw Ste A Vista CA US 92081