| Primary Device ID | 00887868011634 |
| NIH Device Record Key | 7930e6ca-f06b-426a-b6fb-6a1856853b38 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SCREW CORTICAL |
| Version Model Number | 1312-12-115 |
| Catalog Number | 131212115 |
| 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 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 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 | 00887868011634 [Primary] |
| KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-10-24 |
| 00887868011665 | 1312-12-120 |
| 00887868011658 | 1312-12-118 |
| 00887868011641 | 1312-12-116 |
| 00887868011634 | 1312-12-115 |
| 00887868011627 | 1312-12-114 |
| 00887868011610 | 1312-12-113 |
| 00887868011603 | 1312-12-112 |
| 00887868011597 | 1312-12-110 |
| 00887868452772 | 1312-12-112 |
| 00887868452765 | 1312-12-110 |
| 00887868452314 | 1312-12-120 |
| 00887868452307 | 1312-12-118 |
| 00887868452291 | 1312-12-116 |
| 00887868452284 | 1312-12-115 |
| 00887868452277 | 1312-12-114 |
| 00887868452260 | 1312-12-113 |