FDA UDI In Commercial Distribution 🇺🇸 United States

ATEC Porous Ti Interbody System

DI: 00190376116136 · Model: 94133-089 · ALPHATEC SPINE, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ATEC Porous Ti Interbody System
Primary DI
00190376116136
Version / Model
94133-089
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-02
Public Version
1
Public Version Date
2020-03-10
Public Version Status
New
Public Device Record Key
4044bac8-1988-4a78-87ba-0d4afd58f0ba

Device Description

PC Trial, 11 x 10 x 30 - 5°

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
44788 Spinal implant trial

Identifiers

Type ID
Primary 00190376116136

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K183705 000

Device Sizes

Type Value Unit Text
Angle 5 degree
Length 30 Millimeter
Width 10 Millimeter
Height 11 Millimeter