FDA UDI Not in Commercial Distribution 🇺🇸 United States

Insertion Instrument

DI: 81195401178948 · Model: 6130-00 · INTERVENTIONAL SPINE, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Insertion Instrument
Primary DI
81195401178948
Version / Model
6130-00
Catalog Number
6130-00
Company Name
INTERVENTIONAL SPINE, INC
Labeler DUNS
017663522
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-21
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
847424fb-ee27-4afc-97ba-3e1f080c85ee
Distribution End Date
2016-12-23

Device Description

PerX360 System Insertion Tool

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
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 81195401178948

Customer Contacts