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FDA 510(k)

Shockwave Intravascular Lithotripsy (IVL) System with the Javelin Peripheral Intravascular Lithotripsy (IVL) Catheter

K-Number: K242213 · 2024-09-27

Decision Date2024-09-27
Product CodePPN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Shockwave Intravascular Lithotripsy (IVL) System with the Javelin Peripheral Intravascular Lithotripsy (IVL) Catheter is a medical device manufactured by Shockwave Medical, Inc.. It received FDA 510(k) clearance on 2024-09-27 under approval number K242213. The device is classified under product code PPN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Shockwave Intravascular Lithotripsy (IVL) System with the Javelin Peripheral Intravascular Lithotripsy (IVL) Catheter?

Shockwave Intravascular Lithotripsy (IVL) System with the Javelin Peripheral Intravascular Lithotripsy (IVL) Catheter is a medical device that received FDA 510(k) clearance on 2024-09-27. It is manufactured by Shockwave Medical, Inc.. The 510(k) number is K242213.

When was Shockwave Intravascular Lithotripsy (IVL) System with the Javelin Peripheral Intravascular Lithotripsy (IVL) Catheter approved by the FDA?

Shockwave Intravascular Lithotripsy (IVL) System with the Javelin Peripheral Intravascular Lithotripsy (IVL) Catheter received FDA 510(k) clearance on 2024-09-27, under approval number K242213.

What company makes Shockwave Intravascular Lithotripsy (IVL) System with the Javelin Peripheral Intravascular Lithotripsy (IVL) Catheter?

Shockwave Intravascular Lithotripsy (IVL) System with the Javelin Peripheral Intravascular Lithotripsy (IVL) Catheter is manufactured by Shockwave Medical, Inc..

What is the FDA product code for Shockwave Intravascular Lithotripsy (IVL) System with the Javelin Peripheral Intravascular Lithotripsy (IVL) Catheter?

The FDA product code for Shockwave Intravascular Lithotripsy (IVL) System with the Javelin Peripheral Intravascular Lithotripsy (IVL) Catheter is PPN.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.