FDA UDI In Commercial Distribution 🇺🇸 United States

Inertia® Pedicle Screw and Deformity Correxxion® System

DI: 00889929022795 · Model: I10-05-18 · NEXXT SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Inertia® Pedicle Screw and Deformity Correxxion® System
Primary DI
00889929022795
Version / Model
I10-05-18
Company Name
NEXXT SPINE, LLC
Labeler DUNS
003489810
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-26
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
c2730b68-5dcf-4677-9887-58b6b8a8448b

Device Description

Inertia, Iliac Probe, Lenke, Curved, Palm Grip

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 00889929022795

Customer Contacts

Phone
317-436-7801