Easyspine ES9038R
GUDID 03662663036863
LDR Spine Usa, Inc.
Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor Orthopaedic implant impactor| Primary Device ID | 03662663036863 |
| NIH Device Record Key | 707ade6b-a8b0-43cd-adff-46f68ebde575 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Easyspine |
| Version Model Number | ES9038R |
| Catalog Number | ES9038R |
| 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 | 03662663036863 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K121103
FDA Product Code
| NKB | Thoracolumbosacral Pedicle Screw System |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
Moist Heat or Steam Sterilization
[03662663036863]
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 | 2018-12-11 |
On-Brand Devices [Easyspine]
Trademark Results [Easyspine]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 EASYSPINE 78941231 not registered Dead/Abandoned |
ACCO Brands Corporation 2006-07-31 |
 EASYSPINE 78514775 3155009 Live/Registered |
LDR MEDICAL, S.A.S. 2004-11-10 |
 EASYSPINE 77467257 3566916 Live/Registered |
ACCO Brands Corporation 2008-05-06 |
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