NEXGEN®
GUDID 00889024309647
ZIMMER TRABECULAR METAL TECHNOLOGY INC.
Metal-backed patella prosthesis| Primary Device ID | 00889024309647 |
| NIH Device Record Key | 30e6886e-3139-40ea-ae09-6d3f7b9bf454 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NEXGEN® |
| Version Model Number | 00-5876-010-19 |
| Company DUNS | 793120965 |
| Company Name | ZIMMER TRABECULAR METAL 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 | 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
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024309647 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K004013
FDA Product Code
| JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-10-02 |
On-Brand Devices [NEXGEN®]
| 00889024465688 | 00-5879-067-29 |
| 00889024465671 | 00-5879-065-29 |
| 00889024310827 | 00-5987-092-02 |
| 00889024310810 | 00-5887-056-00 |
| 00889024310803 | 00-5887-055-00 |
| 00889024310797 | 00-5887-052-00 |
| 00889024310780 | 00-5887-051-00 |
| 00889024310773 | 00-5887-048-00 |
| 00889024310766 | 00-5887-047-00 |
| 00889024310759 | 00-5887-046-00 |
| 00889024310742 | 00-5887-045-00 |
| 00889024310735 | 00-5887-044-00 |
| 00889024310728 | 00-5887-043-00 |
| 00889024310711 | 00-5886-075-17 |
| 00889024310704 | 00-5886-075-14 |
| 00889024310698 | 00-5886-075-12 |
| 00889024310681 | 00-5886-075-10 |
| 00889024310674 | 00-5886-067-17 |
| 00889024310667 | 00-5886-067-14 |
| 00889024310650 | 00-5886-067-12 |
| 00889024310643 | 00-5886-067-10 |
| 00889024310636 | 00-5886-066-17 |
| 00889024310629 | 00-5886-066-14 |
| 00889024310612 | 00-5886-066-12 |
| 00889024310605 | 00-5886-066-10 |
| 00889024310599 | 00-5886-065-17 |
| 00889024310582 | 00-5886-065-14 |
| 00889024310575 | 00-5886-065-12 |
| 00889024310568 | 00-5886-065-10 |
| 00889024310551 | 00-5886-064-17 |
| 00889024310544 | 00-5886-064-14 |
| 00889024310537 | 00-5886-064-12 |
| 00889024310520 | 00-5886-064-10 |
| 00889024310513 | 00-5886-063-17 |
| 00889024310506 | 00-5886-063-14 |
| 00889024310490 | 00-5886-063-12 |
| 00889024310483 | 00-5886-063-10 |
| 00889024310476 | 00-5886-058-17 |
| 00889024310469 | 00-5886-058-14 |
| 00889024310452 | 00-5886-058-12 |
| 00889024310445 | 00-5886-058-10 |
| 00889024310438 | 00-5886-057-17 |
| 00889024310421 | 00-5886-057-14 |
| 00889024310414 | 00-5886-057-12 |
| 00889024310407 | 00-5886-057-10 |
| 00889024310391 | 00-5886-056-17 |
| 00889024310384 | 00-5886-056-14 |
| 00889024310377 | 00-5886-056-12 |
| 00889024310360 | 00-5886-056-10 |
| 00889024310353 | 00-5886-055-17 |
Trademark Results [NEXGEN]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 NEXGEN 98488003 not registered Live/Pending |
NEXGEN INNOVATION LIMITED 2024-04-08 |
 NEXGEN 98151874 not registered Live/Pending |
NexGen Surveying 2023-08-25 |
 NEXGEN 98124323 not registered Live/Pending |
Cascade Corporation 2023-08-09 |
 NEXGEN 98073423 not registered Live/Pending |
ChlorKing, Inc. 2023-07-06 |
 NEXGEN 97821507 not registered Live/Pending |
Nexgen Global, LLC 2023-03-03 |
 NEXGEN 97821460 not registered Live/Pending |
Nexgen Global, LLC 2023-03-03 |
 NEXGEN 97814118 not registered Live/Pending |
Josh Trujillo 2023-02-27 |
 NEXGEN 97662703 not registered Live/Pending |
Addison HVAC LLC 2022-11-04 |
 NEXGEN 97662699 not registered Live/Pending |
Addison HVAC LLC 2022-11-04 |
 NEXGEN 97390401 not registered Live/Pending |
Easy Automation, Inc. 2022-04-30 |
 NEXGEN 97390400 not registered Live/Pending |
Easy Automation, Inc. 2022-04-30 |
 NEXGEN 97115419 not registered Live/Pending |
DLX Enterprises, LLC 2021-11-09 |
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