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
1596212009
Device Listing 1596212009
Listing Summary
#
Listing key
1596212009
Premarket submission
K242364
Device
IdentiTi™ II Interbody System
Applicant
Alphatec Spine, Inc.
Product code
MAX
Decision date
2024-10-04
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
145220
2027467
2027467
ALPHATEC SPINE, INC.
1
Y
2026-01-01
1950 Camino Vida Roble Carlsbad CA US 92008
295423
3019878714
3019878714
Alphatec Spine, Inc.
1
Y
2026-01-01
4101 Willow Lake Blvd. Memphis TN US 38118