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
1714009337
Device Listing 1714009337
Listing Summary
#
Listing key
1714009337
Premarket submission
K101301
Device
STALIF MIDLINE
Applicant
Centinel Spine
Product code
MAX
Decision date
2010-09-24
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
52461
1225492
3001237338
NextPhase Medical Devices LLC
1
N
2026-01-01
88 Airport Dr ROCHESTER NH US 03867