Marathon Flow Directed Micro Catheter— 510(k) K202318
Substantially EquivalentMicro Therapeutics, Inc. d/b/a ev3 Neurovascular
FDA 510(k) clearance K202318 for Marathon Flow Directed Micro Catheter, Substantially Equivalent on 2020-09-14. Applicant: Micro Therapeutics, Inc. d/b/a ev3 Neurovascular. Device class: 2.
Clearance details
- Applicant
- Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
- Product code
- Code KRA
- Device class
- Class 2
- Regulation
- 21 CFR 870.1210
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Irvine, CA, US
Recent devices under product code KRA
view allMore clearances from Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
view all- K241388 — Rist 079 Radial Access Guide Catheter; Rist 071 Radial Access Guide Catheter; Rist Radial Access Selective Catheter
- K243418 — Riptide Aspiration Pump; Riptide Collection Canister with Intermediate Tubing
- K243080 — Riptide Aspiration System
- K211990 — Rist 071 Radial Access Guide Catheter
- K203432 — Axium Detachable Coil; Axium Prime Detachable Coil
Adverse events under product code KRA
product code KRA- Death
- 234
- Injury
- 1,029
- Malfunction
- 3,012
- Other
- 2
- Total
- 4,277
Source: openFDA MAUDE database, through . 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.