K232290
- 510(k) number
- K232290
- Device name
- INTELLIO SHIFT System
- Applicant
- ArthroCare Corporation TX · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2023-12-11
- Date received
- 2023-08-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 3.2 MB · U.S. public domain
Also available from FDA: K232290.pdf
Official FDA record: K232290
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.