| Primary Device ID | 00887868011856 |
| NIH Device Record Key | 18a8aab4-28bf-4b67-b321-c8119752a290 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | F³®PLATE HIGH FLEX Y |
| Version Model Number | 1312-12-257 |
| Catalog Number | 131212257 |
| 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 | 00887868011856 [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 |