FDA UDI In Commercial Distribution 🇺🇸 United States

IdentiTi

DI: 00811801033902 · Model: CI-10192 · ALPHATEC SPINE, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
IdentiTi
Primary DI
00811801033902
Version / Model
CI-10192
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-19
Public Version
1
Public Version Date
2020-09-28
Public Version Status
New
Public Device Record Key
b1234dc1-238c-4289-9f3d-ab4708c1c000

Device Description

Angled ALIF 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
PHM Intervertebral fusion device with bone graft, thoracic
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
12696 Orthopaedic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 00811801033902

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K183705 000