Turbo-Power Laser Atherectomy Catheter— 510(k) K152181
Substantially EquivalentSpectranetics, Inc.
FDA 510(k) clearance K152181 for Turbo-Power Laser Atherectomy Catheter, Substantially Equivalent on 2015-11-12. Applicant: Spectranetics, Inc..
Clearance details
- Applicant
- Spectranetics, Inc.
- Product code
- Code MCW
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Colorado Springs, CO, US
Adverse events under product code MCW
product code MCW- Death
- 38
- Injury
- 1,386
- Malfunction
- 2,676
- Other
- 2
- Total
- 4,102
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.