| Primary Device ID | 00880304207981 |
| NIH Device Record Key | 5b781829-287e-40fc-b23c-6b9b22411f87 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BIOMET PATELLAR SYSTEM |
| Version Model Number | 11-150862 |
| Catalog Number | 11-150862 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| 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 |
| 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 | 00880304207981 [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 | 2019-10-28 |
| Device Publish Date | 2015-10-24 |
| 00880304240278 | 150808 |
| 00880304240247 | 150804 |
| 00880304240230 | 150802 |
| 00880304208001 | 11-150863 |
| 00880304207981 | 11-150862 |
| 00880304207974 | 11-150861 |
| 00880304207967 | 11-150860 |