FDA UDI In Commercial Distribution 🇺🇸 United States

Salvo® Spine System

DI: 10840642159769 · Model: 10-8425 · Spine Wave, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Salvo® Spine System
Primary DI
10840642159769
Version / Model
10-8425
Catalog Number
10-8425
Company Name
Spine Wave, Inc.
Labeler DUNS
067789763
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-01-24
Public Version
2
Public Version Date
2025-11-20
Public Version Status
Update
Public Device Record Key
36de547f-cac0-4911-932b-498279881523

Device Description

In Situ Bender, Left, 5.5/6.0 mm

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
Yes
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
HXW Bender

GMDN Terms

Code Name
44795 Manual orthopaedic bender, reusable

Identifiers

Type ID
Primary 10840642159769

Customer Contacts

Phone
203-944-9494