| Primary Device ID | 00887868056802 |
| NIH Device Record Key | 2d81eee7-7d8e-478c-bec7-a68799555d69 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 20MM THREAD CANNULATED CANCELLOUS SCREW |
| Version Model Number | 8514-50-036 |
| Catalog Number | 851450036 |
| 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 | 00887868056802 [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 |
| 00887868056970 | 8514-50-100 |
| 00887868056963 | 8514-50-095 |
| 00887868056956 | 8514-50-090 |
| 00887868056949 | 8514-50-085 |
| 00887868056932 | 8514-50-080 |
| 00887868056925 | 8514-50-075 |
| 00887868056918 | 8514-50-070 |
| 00887868056901 | 8514-50-065 |
| 00887868056895 | 8514-50-060 |
| 00887868056888 | 8514-50-055 |
| 00887868056871 | 8514-50-050 |
| 00887868056864 | 8514-50-048 |
| 00887868056857 | 8514-50-046 |
| 00887868056840 | 8514-50-044 |
| 00887868056833 | 8514-50-042 |
| 00887868056826 | 8514-50-040 |
| 00887868056819 | 8514-50-038 |
| 00887868056802 | 8514-50-036 |
| 00887868056796 | 8514-50-034 |
| 00887868056789 | 8514-50-032 |
| 00887868056772 | 8514-50-030 |