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
2047669271
Device Listing 2047669271
Listing Summary
#
Listing key
2047669271
Premarket submission
K133184
Device
ARDIS INTERBODY SYSTEM
Applicant
Zimmer Spine, Inc.
Product code
MAX
Decision date
2014-01-30
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