| Primary Device ID | 00822409006687 |
| NIH Device Record Key | b65e970e-d22b-4eff-a835-15d094c97699 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BKS TriMax |
| Version Model Number | 165-1506 |
| Company DUNS | 876542390 |
| Company Name | Ortho Development Corporation |
| Device Count | 1 |
| DM Exempt | true |
| 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 |
| Phone | +1(801)553-9991 |
| customerservice@odev.com | |
| Phone | +1(801)553-9991 |
| customerservice@odev.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00822409006687 [Primary] |
| JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-12-11 |
| Device Publish Date | 2015-08-31 |
| 00822409031436 | RT Size 7 Femoral CR Nonporous |
| 00822409031429 | LT Size 7 Femoral CR Nonporous |
| 00822409031412 | RT Size 6 Femoral CR Nonporous |
| 00822409031405 | LT Size 6 Femoral CR Nonporous |
| 00822409031399 | RT Size 5 Narrow Femoral CR Nonporous |
| 00822409031382 | LT Size 5 Narrow Femoral CR Nonporous |
| 00822409031375 | RT Size 5 Femoral CR Nonporous |
| 00822409031368 | LT Size 5 Femoral CR Nonporous |
| 00822409031351 | RT Size 4 Narrow Femoral CR Nonporous |
| 00822409031344 | LT Size 4 Narrow Femoral CR Nonporous |
| 00822409031337 | RT Size 4 Femoral CR Nonporous |
| 00822409031320 | LT Size 4 Femoral CR Nonporous |
| 00822409031313 | RT Size 3.5 Femoral CR Nonporous |
| 00822409031306 | LT Size 3.5 Femoral CR Nonporous |
| 00822409031290 | RT Size 3 Femoral CR Nonporous |
| 00822409031283 | LT Size 3 Femoral CR Nonporous |
| 00822409031276 | RT Size 2.5 Femoral CR Nonporous |
| 00822409031269 | LT Size 2.5 Femoral CR Nonporous |
| 00822409031252 | RT Size 2 Femoral CR Nonporous |
| 00822409031245 | LT Size 2 Femoral CR Nonporous |
| 00822409031238 | RT Size 1 Femoral CR Nonporous |
| 00822409031221 | LT Size 1 Femoral CR Nonporous |
| 00822409006724 | RT Size 7 PS Femoral Nonporous |
| 00822409006717 | LT Size 7 PS Femoral Nonporous |
| 00822409006700 | RT Size 6 PS Femoral Nonporous |
| 00822409006694 | LT Size 6 PS Femoral Nonporous |
| 00822409006687 | RT Size 5 Narrow PS Femoral Nonporous |
| 00822409006670 | LT Size 5 Narrow PS Femoral Nonporous |
| 00822409006663 | RT Size 5 PS Femoral Nonporous |
| 00822409006656 | LT Size 5 PS Femoral Nonporous |
| 00822409006649 | RT Size 4 Narrow PS Femoral Nonporous |
| 00822409006632 | LT Size 4 Narrow PS Femoral Nonporous |
| 00822409006625 | RT Size 4 PS Femoral Nonporous |
| 00822409006618 | LT Size 4 PS Femoral Nonporous |
| 00822409006601 | RT Size 3.5 PS Femoral Nonporous |
| 00822409006595 | LT Size 3.5 PS Femoral Nonporous |
| 00822409006588 | RT Size 3 PS Femoral Nonporous |
| 00822409006571 | LT Size 3 PS Femoral Nonporous |
| 00822409006564 | RT Size 2.5 PS Femoral Nonporous |
| 00822409006557 | LT Size 2.5 PS Femoral Nonporous |
| 00822409006540 | RT Size 2 PS Femoral Nonporous |
| 00822409006533 | LT Size 2 PS Femoral Nonporous |
| 00822409006526 | RT Size 1 PS Femoral Nonporous |
| 00822409006519 | LT Size 1 PS Femoral Nonporous |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() BKS TRIMAX 86373511 4805333 Live/Registered |
Ortho Development Corporation 2014-08-21 |