FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Pantheris LV Atherectomy Catheter

K Number: K230005 · Decision Jun 6, 2023
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
145
Applicant Total
25
Review Days
154

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Basic Information

Device Name
Pantheris LV Atherectomy Catheter
K Number
K230005
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4875
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Avinger, Inc.
Date Received
January 3, 2023
Decision Date
June 6, 2023
Product Code
MCW
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MCW Catheter, Peripheral, Atherectomy

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Other Clearances by Avinger, Inc.

K Number Device Name
K230594 Tigereye ST CTO-Crossing Catheter
K212468 Tigereye CTO-Crossing Catheter
K212047 Pantheris System
K201330 Tigereye CTO-Crossing Catheter
K182341 Pantheris SV
K173862 Pantheris System
K172236 Pantheris Catheter (8F), Pantheris Catheter (7F), Lightbox HS Imaging Console, Lightbox Sled
K163264 Pantheris Catheter (8F); Pantheris Cather (7F); Lightbox HS Imaging Console; Lightbox Sled
K162326 Pantheris Catheter, Lightbix HS Imaging Console, Lightbox Sled
K160827 Pantheris Catheter
Search all 25 clearances from Avinger, Inc. →