MotoBAND™ CP Lapidus 7100-LZ18-A
GUDID 00815432026036
The MotoBAND™ CP Lapidus Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. The plates in the system are compatible with the DynaForce HiMAX Superelastic Fixation System.
CROSSROADS EXTREMITY SYSTEMS
Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile| Primary Device ID | 00815432026036 |
| NIH Device Record Key | 42d65136-b71f-4651-8453-f10185e97c1c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MotoBAND™ CP Lapidus |
| Version Model Number | LZ Alpha 18mm |
| Catalog Number | 7100-LZ18-A |
| Company DUNS | 058864308 |
| Company Name | CROSSROADS EXTREMITY SYSTEMS |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| 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 | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com | |
| Phone | 901-221-8406 |
| info@crextremity.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00815432026036 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K173710
FDA Product Code
| HRS | Plate, Fixation, Bone |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-10-01 |
| Device Publish Date | 2018-08-30 |
On-Brand Devices [MotoBAND™ CP Lapidus]
| 00815432026098 | The MotoBAND™ CP Lapidus Implant System is a bone plating system indicated for stabilization a |
| 00815432026074 | The MotoBAND™ CP Lapidus Implant System is a bone plating system indicated for stabilization a |
| 00815432026050 | The MotoBAND™ CP Lapidus Implant System is a bone plating system indicated for stabilization a |
| 00815432026036 | The MotoBAND™ CP Lapidus Implant System is a bone plating system indicated for stabilization a |
Trademark Results [MotoBAND]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MOTOBAND 97221321 not registered Live/Pending |
Motuobang(Beijing)Network Technology Co.,Ltd 2022-01-15 |
 MOTOBAND 87811626 5575462 Live/Registered |
Crossroads Extremity Systems 2018-02-26 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.