Inertia® MIS Pedicle Screw System
GUDID 00889929019146
Inertia MIS Screw Insertion Case
NEXXT SPINE, LLC
Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable| Primary Device ID | 00889929019146 |
| NIH Device Record Key | 5eee3fc0-e8ab-439a-9981-c22121873b29 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Inertia® MIS Pedicle Screw System |
| Version Model Number | C10-01-20 |
| Company DUNS | 003489810 |
| Company Name | NEXXT SPINE, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com | |
| Phone | 317-436-7801 |
| Support@nexxtspine.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889929019146 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K132412
FDA Product Code
| KWP | Appliance, Fixation, Spinal Interlaminal |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
[00889929019146]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2021-07-08 |
| Device Publish Date | 2016-09-24 |
On-Brand Devices [Inertia® MIS Pedicle Screw System]
| 00889929019016 | Screw Loading Guide |
| 00889929019009 | Reducer |
| 00889929018804 | Tower Reattachment Guide |
| 00889929018798 | Tower Attachment Tool |
| 00889929018729 | Percutaneous Tower |
| 00889929018705 | Counter Torque Wrench |
| 00889929018682 | Dilator 2, Radel |
| 00889929019221 | Inertia MIS Reduction Tower Case |
| 00889929019214 | Inertia MIS Compressor/Distractor Case |
| 00889929019207 | Inertia MIS Percutaneous Tower Case |
| 00889929019191 | K-Wire Caddy, Long |
| 00889929019184 | Inertia MIS Rod Manipulation Case |
| 00889929019177 | Inertia MIS Screw Insertion Case |
| 00889929019160 | K-Wire Caddy |
| 00889929019153 | Inertia MIS Rod Manipulation Case |
| 00889929019146 | Inertia MIS Screw Insertion Case |
| 00889929052037 | K-Wire, Nitinol, Blunt Tip, Ø1.4x480mm |
| 00889929052020 | K-Wire, Nitinol, Trocar Tip, Ø1.4x480mm |
| 00889929053799 | K-Wire, Nitinol, Blunt Tip, Ø1.4x590mm |
Trademark Results [Inertia]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 INERTIA 97640508 not registered Live/Pending |
Inertia Inc. 2022-10-20 |
 INERTIA 97263823 not registered Live/Pending |
AETERNA POST PRODUCTION, INC. 2022-02-11 |
 INERTIA 90251251 not registered Live/Pending |
The Carlstar Group LLC 2020-10-13 |
 INERTIA 90109735 not registered Live/Pending |
Inertia LLC 2020-08-12 |
 INERTIA 88668380 not registered Live/Pending |
Elite Tackle Group, LLC 2019-10-25 |
 INERTIA 88291597 not registered Live/Pending |
Dick's Sporting Goods, Inc. 2019-02-06 |
 INERTIA 87764186 not registered Dead/Abandoned |
Elite Tackle Group LLC 2018-01-22 |
 INERTIA 87374452 not registered Dead/Abandoned |
Bushnell Inc. 2017-03-16 |
 INERTIA 86501465 not registered Dead/Abandoned |
Buck Knives, Inc. 2015-01-12 |
 INERTIA 86446381 4882832 Live/Registered |
Michael Zubi 2014-11-06 |
 INERTIA 86445762 not registered Dead/Abandoned |
FREE COUNTRY, LTD 2014-11-05 |
 INERTIA 86322579 4688188 Live/Registered |
Wineman Technology Inc. 2014-06-27 |
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