| Primary Device ID | 00850696006691 |
| NIH Device Record Key | 65e49dd4-9fb4-424a-95dc-346ce09ec852 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SpineSTAR Ablation Instrument (10|15, Short) |
| Version Model Number | 3192 |
| Catalog Number | 3192 |
| Company DUNS | 169957607 |
| Company Name | Dfine, 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 | 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 | 00850696006691 [Primary] |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-03-19 |
| Device Publish Date | 2016-08-23 |
| 00850696006004 - SpineSTAR Ablation Instrument (10|15, Long) | 2020-03-19 |
| 00850696006011 - SpineSTAR Ablation Instrument (5|10, Long) | 2020-03-19 |
| 00850696006028 - StabiliT Bone Cement and Saturate Mixing System | 2020-03-19 |
| 00850696006073 - StabiliT VP Fracture Kit | 2020-03-19 |
| 00850696006226 - StabiliT First Fracture Kit | 2020-03-19 |
| 00850696006233 - StabiliT First Fracture Kit | 2020-03-19 |
| 00850696006240 - STAR Tumor Ablation Kit (10|15, Short) with PowerCURVE | 2020-03-19 ala carte packaging |
| 00850696006257 - STAR Tumor Ablation Kit (5|10, Long) with PowerCURVE | 2020-03-19 ala carte packaging |