| Primary Device ID | 00887868053481 |
| NIH Device Record Key | e7e398e8-bc84-4123-ae46-b9a70fcbff01 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CANNULATED FULLY THREADED CANCELLOUS SCREW, REDUCED HEAD |
| Version Model Number | 8502-48-028 |
| Catalog Number | 850248028 |
| 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 | 00887868053481 [Primary] |
| HWC | Screw, fixation, bone |
| 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 |
| 00887868053634 | 8502-48-070 |
| 00887868053627 | 8502-48-065 |
| 00887868053610 | 8502-48-060 |
| 00887868053603 | 8502-48-055 |
| 00887868053597 | 8502-48-050 |
| 00887868053580 | 8502-48-048 |
| 00887868053573 | 8502-48-046 |
| 00887868053566 | 8502-48-044 |
| 00887868053559 | 8502-48-042 |
| 00887868053542 | 8502-48-040 |
| 00887868053535 | 8502-48-038 |
| 00887868053528 | 8502-48-036 |
| 00887868053511 | 8502-48-034 |
| 00887868053504 | 8502-48-032 |
| 00887868053498 | 8502-48-030 |
| 00887868053481 | 8502-48-028 |
| 00887868053474 | 8502-48-026 |
| 00887868053467 | 8502-48-024 |
| 00887868053450 | 8502-48-022 |
| 00887868053443 | 8502-48-020 |
| 00887868053436 | 8502-48-018 |
| 00887868053429 | 8502-48-016 |
| 00887868053412 | 8502-48-014 |
| 00887868053405 | 8502-48-012 |
| 00887868053399 | 8502-48-010 |