RADIUS MICRO SNARE— 510(k) K022201

Name: FDA 510(k) clearance K022201
Creator: U.S. Food and Drug Administration
Published: 2003-02-03

Substantially Equivalent

Radius Medical Technologies, Inc.

FDA 510(k) clearance K022201 for RADIUS MICRO SNARE, Substantially Equivalent on 2003-02-03. Applicant: Radius Medical Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Radius Medical Technologies, Inc.
Product code: Code MMX
Device class: Class 2
Regulation: 21 CFR 870.5150
Advisory panel: Cardiovascular
Date received: 2002-07-05
Decision date: 2003-02-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hopkonton, MA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Radius Medical Technologies, Inc.

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K070502 — RADIUS SNARE2007-10-04
K071457 — MODIFICATION TO RADIUS SNARE2007-09-25
K032899 — RADIUS COUGAR WIRE2003-10-17
K032129 — RADIUS 018 COUGAR WIRE2003-07-17
K021441 — RADIUS SNARE2002-06-14

Adverse events under product code MMX

product code MMX

Death: 3
Total: 3

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. 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.