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
1319564844
Device Listing 1319564844
Listing Summary
#
Listing key
1319564844
Premarket submission
P050010
Device
PRODISC -L TOTAL DISC REPLACEMENT DEVICE
Applicant
Centinel Spine, LLC
Product code
MJO
Decision date
2006-08-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
92930
3007494564
3007494564
CENTINEL SPINE, LLC
1
N
2026-01-01
900 Airport Rd Ste 3B West Chester PA US 19380