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
1353913725
Device Listing 1353913725
Listing Summary
#
Listing key
1353913725
Premarket submission
K131156
Device
LANX SPINAL FIXATION SYSTEM
Applicant
Lanx, Inc.
Product code
KWP
Decision date
2013-05-24
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
131629
3009174179
3009174179
ZIMMER BIOMET SPINE. INC
1
Y
2020-04-25
5400 Meltech Blvd Ste 119 Memphis TN US 38118