| Primary Device ID | 00841036190224 |
| NIH Device Record Key | 79694ddb-1d5c-4e36-a06d-ab9979d392eb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | STERNALOCK 360 SYSTEM |
| Version Model Number | 74-0014 |
| Catalog Number | 74-0014 |
| Company DUNS | 046189866 |
| Company Name | BIOMET MICROFIXATION, INC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00841036190224 [Primary] |
| HRS | Plate, 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 | 2015-11-17 |
| 00841036192136 | 74-1192 |
| 00841036275273 | 74-1193 |
| 00841036275266 | 74-1192 |
| 00841036202484 | 74-1195 |
| 00841036192143 | 74-1193 |
| 00841036190668 | 74-0004 |
| 00841036190231 | 74-0016 |
| 00841036190224 | 74-0014 |
| 00841036190217 | 74-0012 |
| 00841036190200 | 74-0010 |
| 00841036190026 | 74-0002 |
| 00841036190019 | 74-0003 |
| 00888233026604 | 74-0004 |
| 00888233026598 | 74-0003 |
| 00888233026581 | 74-0002 |