FDA UDI In Commercial Distribution 🇺🇸 United States

Ascend

DI: 00190376517964 · Model: 156-12-250 · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Ascend
Primary DI
00190376517964
Version / Model
156-12-250
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-10-28
Public Version
2
Public Version Date
2025-04-30
Public Version Status
Update
Public Device Record Key
d9ff7444-35d1-4302-8b3b-40b183416aef

Device Description

CV VBR 12 mm Expansion Driver Long

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
PLR Spinal vertebral body replacement device - Cervical

GMDN Terms

Code Name
12696 Orthopaedic inorganic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 00190376517964

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K232173 000