FDA UDI In Commercial Distribution 🇺🇸 United States

IdentiTi II

DI: 00190376679990 · Model: 832-07342810-S · ALPHATEC SPINE, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
IdentiTi II
Primary DI
00190376679990
Version / Model
832-07342810-S
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-08
Public Version
1
Public Version Date
2025-09-16
Public Version Status
New
Public Device Record Key
5a1360f0-b968-4891-bdb4-7a6e21bfb971

Device Description

IDENTITI II ALIF SA 7 x 34 x 28 mm, 10°

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral fusion device with bone graft, lumbar
OVD Intervertebral fusion device with integrated fixation, lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 00190376679990

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K251575 000

Device Sizes

Type Value Unit Text
Width 34 Millimeter
Depth 28 Millimeter
Height 7 Millimeter
Angle 10 degree