FDA UDI In Commercial Distribution 🇺🇸 United States

Inertia® Pedicle Screw System

DI: 00889929006184 · Model: 10-4-001 · 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
00889929006184
Version / Model
10-4-001
Company Name
NEXXT SPINE, LLC
Labeler DUNS
003489810
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-10
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
0426bfb9-47a8-40f8-a001-f9337d169bba

Device Description

Set Screw, Revision

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
Yes
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
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation

GMDN Terms

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

Identifiers

Type ID
Primary 00889929006184

Customer Contacts

Phone
317-436-7801

Premarket Submissions

Submission Number Supplement Number
K090984 000

Device Sizes

Type Value Unit Text
Outer Diameter 10.5 Millimeter
Length 4.25 Millimeter