FDA UDI In Commercial Distribution 🇺🇸 United States

Inertia® Pedicle Screw System

DI: 00889929005262 · Model: 10-17-5595 · NEXXT SPINE, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Inertia® Pedicle Screw System
Primary DI
00889929005262
Version / Model
10-17-5595
Company Name
NEXXT SPINE, LLC
Labeler DUNS
003489810
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-08
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
02c0d8e1-ce0f-48f1-b8ec-99e06c786488

Device Description

MIS Rod, Curved, Ø5.5mm x 95mm

Device Characteristics

Single Use
Yes
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
No
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
MNI Orthosis, Spinal Pedicle Fixation
MNH Orthosis, Spondylolisthesis Spinal Fixation

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 00889929005262

Customer Contacts

Phone
317-436-7801

Premarket Submissions

Submission Number Supplement Number
K090984 000

Device Sizes

Type Value Unit Text
Outer Diameter 5.5 Millimeter
Length 95 Millimeter
Device Size Text, specify MIS