| Primary Device ID | 00887868056673 |
| NIH Device Record Key | 16b51db5-58c3-4f24-8aff-2c209204c096 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CANNULATED CORTICAL LAG SCREW |
| Version Model Number | 8514-48-140 |
| Catalog Number | 851448140 |
| 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 Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868056673 [Primary] |
| HSB | ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES |
| 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 |
| 00887868007705 | 14250-70 |
| 00887868007699 | 14250-65 |
| 00887868007682 | 14250-60 |
| 00887868007675 | 14250-55 |
| 00887868007668 | 14250-50 |
| 00887868007651 | 14250-48 |
| 00887868007644 | 14250-46 |
| 00887868007637 | 14250-44 |
| 00887868007620 | 14250-42 |
| 00887868007613 | 14250-40 |
| 00887868007606 | 14250-38 |
| 00887868007590 | 14250-36 |
| 00887868007583 | 14250-34 |
| 00887868007576 | 14250-32 |
| 00887868007569 | 14250-30 |
| 00887868056765 | 8514-48-170 |
| 00887868056758 | 8514-48-165 |
| 00887868056741 | 8514-48-160 |
| 00887868056734 | 8514-48-155 |
| 00887868056727 | 8514-48-150 |
| 00887868056710 | 8514-48-148 |
| 00887868056703 | 8514-48-146 |
| 00887868056697 | 8514-48-144 |
| 00887868056680 | 8514-48-142 |
| 00887868056673 | 8514-48-140 |
| 00887868056666 | 8514-48-138 |
| 00887868056659 | 8514-48-136 |
| 00887868056642 | 8514-48-134 |
| 00887868056635 | 8514-48-132 |
| 00887868056628 | 8514-48-130 |