SIDEKICK
GUDID 00840420128652
WRIGHT MEDICAL TECHNOLOGY, INC.
External orthopaedic fixation system, reusable| Primary Device ID | 00840420128652 |
| NIH Device Record Key | 54d90943-3929-4afa-b41e-b6bd0311e6fb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SIDEKICK |
| Version Model Number | RR5040 |
| Company DUNS | 807201207 |
| Company Name | WRIGHT MEDICAL TECHNOLOGY, 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com |
Device Dimensions
| Length | 180 Millimeter |
| Outer Diameter | 5 Millimeter |
| Length | 180 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 5 Millimeter |
| Length | 180 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 5 Millimeter |
| Length | 180 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 5 Millimeter |
| Length | 180 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 5 Millimeter |
| Length | 180 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 5 Millimeter |
| Length | 180 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 5 Millimeter |
| Length | 180 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 5 Millimeter |
| Length | 180 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 5 Millimeter |
| Length | 180 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 5 Millimeter |
| Length | 180 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 5 Millimeter |
| Length | 180 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 5 Millimeter |
| Length | 180 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 5 Millimeter |
| Length | 180 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 5 Millimeter |
| Length | 180 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 5 Millimeter |
| Length | 180 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 5 Millimeter |
| Length | 180 Millimeter |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840420128652 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K043174
FDA Product Code
| KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00840420128652]
Moist Heat or Steam Sterilization
[00840420128652]
Moist Heat or Steam Sterilization
[00840420128652]
Moist Heat or Steam Sterilization
[00840420128652]
Moist Heat or Steam Sterilization
[00840420128652]
Moist Heat or Steam Sterilization
[00840420128652]
Moist Heat or Steam Sterilization
[00840420128652]
Moist Heat or Steam Sterilization
[00840420128652]
Moist Heat or Steam Sterilization
[00840420128652]
Moist Heat or Steam Sterilization
[00840420128652]
Moist Heat or Steam Sterilization
[00840420128652]
Moist Heat or Steam Sterilization
[00840420128652]
Moist Heat or Steam Sterilization
[00840420128652]
Moist Heat or Steam Sterilization
[00840420128652]
Moist Heat or Steam Sterilization
[00840420128652]
Moist Heat or Steam Sterilization
[00840420128652]
Moist Heat or Steam Sterilization
[00840420128652]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-10-01 |
On-Brand Devices [SIDEKICK]
Trademark Results [SIDEKICK]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SIDEKICK 98762733 not registered Live/Pending |
Mej Consulting LLC 2024-09-21 |
 SIDEKICK 98709478 not registered Live/Pending |
SIER TECHNOLOGIES LLC 2024-08-21 |
 SIDEKICK 98606057 not registered Live/Pending |
WWBD SOLUTIONS INC. 2024-06-18 |
 SIDEKICK 98539996 not registered Live/Pending |
AMG LAB LLC 2024-05-08 |
 SIDEKICK 98524723 not registered Live/Pending |
Sense It LLC 2024-04-29 |
 SIDEKICK 98349207 not registered Live/Pending |
Sidekick Enterprises, Inc. 2024-01-09 |
 SIDEKICK 98290315 not registered Live/Pending |
Lance Dewbre, 2023-11-29 |
SIDEKICK 98290315 not registered Live/Pending |
Dewbre, Bill 2023-11-29 |
 SIDEKICK 98142191 not registered Live/Pending |
The Nanny Network, LLC 2023-08-21 |
 SIDEKICK 98141743 not registered Live/Pending |
The Nanny Network, LLC 2023-08-21 |
 SIDEKICK 98141724 not registered Live/Pending |
The Nanny Network, LLC 2023-08-21 |
 SIDEKICK 98027511 not registered Live/Pending |
Dew Beauty Inc. 2023-06-05 |
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