FDA UDI In Commercial Distribution 🇺🇸 United States

IdentiTi

DI: 00811801034114 · Model: CI-10392-14-04186010 · ALPHATEC SPINE, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
IdentiTi
Primary DI
00811801034114
Version / Model
CI-10392-14-04186010
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
6fb428f6-53b7-4f03-83c1-b504075fbba0

Device Description

LIF TRIAL, OFFSET LEFT, 4 x 18 x 60 mm, 10°

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
44788 Spinal implant trial

Identifiers

Type ID
Primary 00811801034114

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K183705 000

Device Sizes

Type Value Unit Text
Height 4 Millimeter
Width 18 Millimeter
Depth 60 Millimeter
Angle 10 degree