FDA UDI In Commercial Distribution 🇺🇸 United States

IdentiTi

DI: 00190376198538 · Model: 122-08103510-S · ALPHATEC SPINE, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
IdentiTi
Primary DI
00190376198538
Version / Model
122-08103510-S
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-01-10
Public Version
2
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
8b4cf7b6-2d53-400f-af11-828220917a6d

Device Description

IDENTITi PC POROUS Ti SPACER, 8 x 10 x 35 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
Yes
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
PHM Intervertebral fusion device with bone graft, thoracic

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 00190376198538

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K183705 000

Device Sizes

Type Value Unit Text
Width 10 Millimeter
Angle 10 degree
Height 8 Millimeter
Length 35 Millimeter