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
1419703530
Device Listing 1419703530
Listing Summary
#
Listing key
1419703530
Premarket submission
K180814
Device
CoreLink® M3 Stand-Alone Anterior Lumbar System
Applicant
Corelink, LLC
Product code
OVD
Decision date
2018-08-10
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
210005
3008583793
3008583793
ZAVATION
1
N
2026-01-01
3670 Flowood Dr Flowood MS US 39232