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
1093931863
Device Listing 1093931863
Listing Summary
#
Listing key
1093931863
Premarket submission
K073144
Device
LANX INTERVERTEBRAL BODY FUSION DEVICE
Applicant
Lanx, LLC
Product code
MAX
Decision date
2008-01-24
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