| Primary Device ID | 00887868011795 |
| NIH Device Record Key | 79ed64cb-bef2-4131-9588-b84bc8b6ed2d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | F³®PLATE HIGH STRENGTH LEFT |
| Version Model Number | 1312-12-251 |
| Catalog Number | 131212251 |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868011795 [Primary] |
| HRS | PLATE, FIXATION, BONE |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-01-14 |
| Device Publish Date | 2015-10-24 |
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| 00887868578250 - Comprehensive® | 2024-11-13 |
| 08428898885684 - BIPASS DISPOSABLE PUSHER | 2024-09-11 |
| 08428898885691 - BIPASS DISPOSABLE PUSHER | 2024-09-11 |
| 00880304338548 - AGC ANTERIOR FILE | 2024-09-11 |
| 00880304339224 - PARALLEL PULLER | 2024-09-11 |
| 00880304342187 - AGC MODULAR TIBIAL II | 2024-09-11 |
| 00880304365247 - BIO-MODULAR | 2024-09-11 |