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
2034009110
Device Listing 2034009110
Listing Summary
#
Listing key
2034009110
Premarket submission
K051027
Device
STALIF TT
Applicant
Surgicraft , Ltd.
Product code
MQP
Decision date
2005-06-29
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