| Primary Device ID | M97032000170600 |
| NIH Device Record Key | 0a81fbfc-1748-4160-8bf9-656e422e6f34 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DynaNail Helix, Headless, 60mm |
| Version Model Number | 3200-01-7060 |
| Company DUNS | 601306413 |
| Company Name | Medshape, Inc. |
| 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 | false |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |