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
1551728502
Device Listing 1551728502
Listing Summary
#
Listing key
1551728502
Premarket submission
K121136
Device
RENOIR POSTERIOR CERVIAL FIXATION SYSTEM
Applicant
Accel Spine
Product code
KWP
Decision date
2012-08-09
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
190664
3009051471
3009051471
CTL Medical Corporation
1
N
2026-01-01
2052 McKenzie Drive, Building 1 Carrollton TX US 75006