| Primary Device ID | 00880304510098 |
| NIH Device Record Key | 2ed3e0b2-7c57-4d6d-b34a-d9803b6d8053 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Oxford Partial Knee System |
| Version Model Number | 42-411441 |
| Catalog Number | 42-411441 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304510098 [Primary] |
| NRA | Prosthesis, Knee, Femorotibial, Unicompartmental, Semi-Constrained, Metal/Polymer, Mobile Bearing |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
[00880304510098]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2014-08-29 |
| 00880304512047 | Right Medial Tibial Alignment |
| 00880304511804 | Left Medial Tibial Alignment |
| 00880304510227 | Signature Femoral Drill Guide |
| 00880304510210 | Signature Femoral Drill Guide |
| 00880304510203 | Signature Femoral Drill Guide |
| 00880304510197 | Signature Tibial Drill Guide |
| 00880304510180 | Signature Femoral Drill Guide |
| 00880304510173 | Signature Femoral Drill Guide |
| 00880304510166 | Signature Femoral Drill Guide |
| 00880304510159 | Signature Femoral Drill Guide |
| 00880304510142 | Signature Femoral Drill Guide |
| 00880304510135 | Signature Femoral Drill Guide |
| 00880304510128 | Signature Femoral Drill Guide |
| 00880304510111 | Signature Femoral Drill Guide |
| 00880304510104 | Signature Femoral Drill Guide |
| 00880304510098 | Signature Femoral Drill Guide |