| Primary Device ID | 08806390883702 | 
| NIH Device Record Key | 09bd2b6f-e4b8-4931-90bf-6288fe5e8c1d | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Summa Orthopaedics System Surgical Instrument | 
| Version Model Number | SO-112-120 | 
| Company DUNS | 688811603 | 
| Company Name | Jeil Medical Corporation | 
| 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 | 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 |