FDA UDI In Commercial Distribution 🇺🇸 United States

Salvo® Spine System

DI: 10840642159677 · Model: 10-8388 · Spine Wave, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Salvo® Spine System
Primary DI
10840642159677
Version / Model
10-8388
Catalog Number
10-8388
Company Name
Spine Wave, Inc.
Labeler DUNS
067789763
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-14
Public Version
1
Public Version Date
2023-07-24
Public Version Status
New
Public Device Record Key
b206ad21-e6c1-462c-afd8-f31c35fbe2ca

Device Description

Screwdriver, Reduction Screw, 5.5/6.0 mm, T25

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
HXX Screwdriver

GMDN Terms

Code Name
33968 Surgical screwdriver, reusable

Identifiers

Type ID
Primary 10840642159677

Customer Contacts

Phone
203-944-9494