VerteFIT VF9109R
GUDID 03662663033206
LDR Spine Usa, Inc.
Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal Orthopaedic surgical distractor, internal| Primary Device ID | 03662663033206 |
| NIH Device Record Key | 0b618351-a71c-48c8-9b54-d0536dfd170b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VerteFIT |
| Version Model Number | VF9109R |
| Catalog Number | VF9109R |
| Company DUNS | 615789729 |
| Company Name | LDR Spine Usa, Inc. |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com | |
| Phone | 800-699-3360 |
| custserv@ldrspine.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03662663033206 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K162133
FDA Product Code
| MQP | Spinal Vertebral Body Replacement Device |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
[03662663033206]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2022-03-10 |
| Device Publish Date | 2018-12-12 |
On-Brand Devices [VerteFIT]
| 03662663033282 | VF9117R |
| 03662663033275 | VF9116R |
| 03662663033114 | VF9012R |
| 03662663036184 | VF3102T |
| 03662663036177 | VF2102T |
| 03662663036160 | VF1102T |
| 03662663049290 | VF991C-CR |
| 03662663049283 | VF991B-CR |
| 03662663049276 | VF991A-CR |
| 03662663049238 | VF990-CR |
| 03662663036153 | VF9192R |
| 03662663036146 | VF9191R |
| 03662663036139 | VF9190R |
| 03662663035422 | VF9118R |
| 03662663035170 | VF9013R |
| 03662663033268 | VF9115R |
| 03662663033213 | VF9110R |
| 03662663033206 | VF9109R |
| 03662663033190 | VF9108R |
| 03662663033183 | VF9107R |
| 03662663033107 | VF9011R |
| 03662663033077 | VF9008R |
| 03662663033060 | VF9007R |
| 03662663033053 | VerteFIT |
Trademark Results [VerteFIT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VERTEFIT 86539376 not registered Dead/Abandoned |
LDR Medical, S.A.S. 2015-02-19 |
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