INTERCEPTOR PLUS CORONARY FILTER SYSTEMS— 510(k) K073523

Name: FDA 510(k) clearance K073523
Creator: U.S. Food and Drug Administration
Published: 2008-08-01

Substantially Equivalent

Medtronic, Inc.

FDA 510(k) clearance K073523 for INTERCEPTOR PLUS CORONARY FILTER SYSTEMS, Substantially Equivalent on 2008-08-01. Applicant: Medtronic, Inc.. Device class: 2.

Clearance details

Applicant: Medtronic, Inc.
Product code: Code NFA
Device class: Class 2
Regulation: 21 CFR 870.1250
Advisory panel: Cardiovascular
Date received: 2007-12-14
Decision date: 2008-08-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Danvers, MA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code NFA

view all

K073563 — MODIFICATION TO PROXIS SYSTEM2008-01-31
K063785 — SPIDERFX EMBOLIC PROTECTION DEVICE2007-01-19
K062870 — TRIACTIV FX EMBOLIC PROTECTION SYSTEM, MODEL PN 60040-02; -032006-10-20
K060651 — PROXIS SYSTEM, MODEL EPS1012006-09-13
K052523 — PROXIS SYSTEM2006-09-07

More clearances from Medtronic, Inc.

view all

K262735 — LINQ II Insertable Cardiac Monitor (ICM) (LNQ22)2026-08-28
K262005 — Affera Integrated Mapping System2026-08-21
K261335 — VitalFlow Set with Balance Biosurface2026-07-31
K261866 — Concerto Versa Detachable Coil2026-06-24
K260195 — Elongated One-Piece Arterial (EOPA) 3D Arterial Cannulae2026-04-23

Data sourced from openFDA. This site is unofficial and independent of the FDA.