| Primary Device ID | 00887868012051 |
| NIH Device Record Key | 23145bbc-506f-409d-babb-7e1935e037ac |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MULTI-DIRECTIONAL THREADED PEG |
| Version Model Number | 1312-12-420 |
| Catalog Number | 131212420 |
| 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 | 00887868012051 [Primary] |
| LXT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE |
| 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 |
| 00887868012105 | 1312-12-430 |
| 00887868012099 | 1312-12-428 |
| 00887868012082 | 1312-12-426 |
| 00887868012075 | 1312-12-424 |
| 00887868012068 | 1312-12-422 |
| 00887868012051 | 1312-12-420 |
| 00887868012044 | 1312-12-418 |
| 00887868012037 | 1312-12-416 |
| 00887868012020 | 1312-12-415 |
| 00887868012013 | 1312-12-414 |
| 00887868012006 | 1312-12-413 |
| 00887868011993 | 1312-12-412 |
| 00887868011986 | 1312-12-411 |
| 00887868011979 | 1312-12-410 |
| 00887868452598 | 1312-12-430 |
| 00887868452581 | 1312-12-428 |
| 00887868452574 | 1312-12-426 |
| 00887868452567 | 1312-12-424 |
| 00887868452550 | 1312-12-422 |
| 00887868452543 | 1312-12-420 |
| 00887868449864 | 1312-12-418 |
| 00887868449857 | 1312-12-416 |
| 00887868449840 | 1312-12-415 |
| 00887868449833 | 1312-12-414 |
| 00887868449826 | 1312-12-413 |
| 00887868449819 | 1312-12-412 |
| 00887868449802 | 1312-12-411 |
| 00887868449796 | 1312-12-410 |