FDA UDI In Commercial Distribution 🇺🇸 United States

Ascend

DI: 00190376670591 · Model: 157-PRO-12L-225005-S · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ascend
Primary DI
00190376670591
Version / Model
157-PRO-12L-225005-S
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-21
Public Version
1
Public Version Date
2025-10-29
Public Version Status
New
Public Device Record Key
de8d0a6e-f1a7-46cf-8771-4f98e6972f88

Device Description

12mm CORE, NANOTEC LAT 22 x 50 mm 5°

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
No
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
MQP Spinal vertebral body replacement device

GMDN Terms

Code Name
34170 Vertebral body prosthesis

Identifiers

Type ID
Primary 00190376670591

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K232173 000

Device Sizes

Type Value Unit Text
Width 22 Millimeter
Length 50 Millimeter
Angle 5 degree