| Primary Device ID | 00887868251856 |
| NIH Device Record Key | 23acd72c-f2f2-49f2-bfb0-6d58f9bb9788 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | OSS™ Orthopedic Salvage System |
| Version Model Number | CP102848 |
| Catalog Number | CP102848 |
| 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 |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868251856 [Primary] |
| KRO | PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2018-05-29 |
| 00887868267253 | 151871 |
| 00887868267246 | 151870 |
| 00887868267239 | 151869 |
| 00887868267222 | 151868 |
| 00887868267215 | 151867 |
| 00887868267208 | 151866 |
| 00887868267192 | 151865 |
| 00887868267185 | 151864 |
| 00887868267178 | 151863 |
| 00887868267161 | 151862 |
| 00887868267154 | 151861 |
| 00887868251856 | CP102848 |
| 00887868251849 | CP102847 |
| 00887868251832 | CP102846 |
| 00887868251825 | CP102845 |
| 00887868251818 | CP102844 |
| 00887868251801 | CP102843 |
| 00887868251795 | CP102840 |
| 00887868251788 | CP102839 |
| 00887868251771 | CP102838 |
| 00880304240056 | 150489 |