FDA UDI In Commercial Distribution 🇺🇸 United States

IdentiTi II

DI: 00190376694405 · Model: 801-240 · ALPHATEC SPINE, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
IdentiTi II
Primary DI
00190376694405
Version / Model
801-240
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-02-18
Public Version
1
Public Version Date
2026-02-26
Public Version Status
New
Public Device Record Key
ef1b87b9-888c-423b-acf5-d03bd6b3d792

Device Description

IDTi II LIF Angled Inserter

Device Characteristics

Single Use
No
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MAX Intervertebral fusion device with bone graft, lumbar
PHM Intervertebral fusion device with bone graft, thoracic

GMDN Terms

Code Name
12696 Orthopaedic inorganic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 00190376694405

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K242364 000