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
1192609008
Device Listing 1192609008
Listing Summary
#
Listing key
1192609008
Premarket submission
K181621
Device
Stable-C Interbody System
Applicant
Nexus Spine, LLC
Product code
OVE
Decision date
2018-10-19
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
112136
3008236846
3008236846
KEYSTONE MANUFACTURING
1
N
2026-01-01
6387 Technology Ave Ste B Kalamazoo MI US 49009