Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Pantheris LV Atherectomy Catheter

K-Number: K230005 · 2023-06-06

ApplicantAvinger, Inc.
Decision Date2023-06-06
Product CodeMCW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Pantheris LV Atherectomy Catheter is a medical device manufactured by Avinger, Inc.. It received FDA 510(k) clearance on 2023-06-06 under approval number K230005. The device is classified under product code MCW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Pantheris LV Atherectomy Catheter?

Pantheris LV Atherectomy Catheter is a medical device that received FDA 510(k) clearance on 2023-06-06. It is manufactured by Avinger, Inc.. The 510(k) number is K230005.

When was Pantheris LV Atherectomy Catheter approved by the FDA?

Pantheris LV Atherectomy Catheter received FDA 510(k) clearance on 2023-06-06, under approval number K230005.

What company makes Pantheris LV Atherectomy Catheter?

Pantheris LV Atherectomy Catheter is manufactured by Avinger, Inc..

What is the FDA product code for Pantheris LV Atherectomy Catheter?

The FDA product code for Pantheris LV Atherectomy Catheter is MCW.

Other Devices by Avinger, Inc.

View all 12 devices →

Related Devices (Code: MCW)

Official Source

View on FDA Database →

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