FDA UDI Not in Commercial Distribution 🇺🇸 United States

Sternal Cable System

DI: 00846468041007 · Model: 402-522 · Pioneer Surgical Technology, 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
Sternal Cable System
Primary DI
00846468041007
Version / Model
402-522
Company Name
Pioneer Surgical Technology, Inc.
Labeler DUNS
793384496
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-01-09
Public Version
8
Public Version Date
2026-01-21
Public Version Status
Update
Public Device Record Key
39a91e21-bcbd-42ed-a909-6f22a937a4e3
Distribution End Date
2025-04-09

Device Description

SS Blunt Needle, 1 Cable Per Pouch

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JDQ Cerclage, Fixation

GMDN Terms

Code Name
44797 Internal spinal fixation system cable

Identifiers

Type ID
Primary 00846468041007

Customer Contacts