| Primary Device ID | 08806390883672 |
| NIH Device Record Key | df5416ff-a9b0-4702-8311-a5c16b00dd62 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Summa Orthopaedics System Surgical Instrument |
| Version Model Number | SO-113-HF-617 |
| Company DUNS | 688811603 |
| Company Name | Jeil Medical Corporation |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |