ARTHROCARE ENT PLASMA WAND
FDA 510(k) clearance K070374 · decided 2007-04-25
Clearance details
- K-number
- K070374
- Device name
- ARTHROCARE ENT PLASMA WAND
- Applicant
- Arthrocare Corp.
- Decision
- Substantially Equivalent
- Date received
- 2007-02-08
- Decision date
- 2007-04-25
- Days to decision
- 76 days
- Clearance type
- Traditional
- Product code
- GEI
- Device class
- 2
- Regulation number
- 878.4400
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Sunnyvale, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| EVac 70 XTRA with Integrated Cable and PROcise EZ View with Integrated Cable Product Usage recall (Z-2105-2015) | ArthroCare Corporation | 2015-07-18 |