Aln Optional Vana Cava Filter

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K113124 ↗

FDA Product Code

DTK

Device Class

Class II

Regulation

21 CFR Part 870.3375

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Aln Optional Vena Cava Filter-Femoral Approach, Jugular Approach, Brachial Approach, Extraction Kit, Precurved Extractio

  Class II

  CE/MDR FDA 510(k) K070514 Active Cleared 30 Jan 2008

• ALN Optional Vena Cava Filter - Femoral Approach, ALN Optional Vena Cava Filter - Jugular Approach, ALN Optional Vena Cava Filter - Brachial Approach, ALN Optional Vena Cava Filter - Femoral Approach with Hook

  Class II

  CE/MDR FDA 510(k) K163699 Active Cleared 8 Sep 2017