ArthroCare Corporation · Class II · Cleared Jan 15, 2016
| K-number | K153675 |
| Device name | Paragon T2 Wand with Integrated Cable |
| Applicant | ArthroCare Corporation |
| Product code | GEI |
| Device class | Class II |
| Decision date | Jan 15, 2016 |
| Decision | Substantially Equivalent |
| Regulation | — |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov