Shockwave Medical Peripheral Intravascular Lithotripsy (IVL) System— 510(k) K221041

Substantially Equivalent

Shockwave Medical, Inc.

FDA 510(k) clearance K221041 for Shockwave Medical Peripheral Intravascular Lithotripsy (IVL) System, Substantially Equivalent on 2022-04-25. Applicant: Shockwave Medical, Inc.. Device class: 2.

Clearance details

Applicant
Shockwave Medical, Inc.
Product code
Code PPN
Device class
Class 2
Regulation
21 CFR 870.1250
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Santa Clara, CA, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code PPN

product code PPN
Death
16
Total
16

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.