# K024349: Aesulap Kopitnik Avm Microclips and Applier

- Pathway: 510(k) (Traditional)
- Applicant: Aesculap, Inc.
- Decided: Mar 24, 2003 after 84 days
- Product code: HCH (Clip, Aneurysm)
- Device class: 2
- Regulation: 21 CFR 882.5200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Aesculap currently marketed Aneurysm Clips and Appliers: named in the summary without a submission number
- (no number) Sugita AVM Microclips: named in the summary without a submission number

## Indications for use
The Aesculap AVM Microclips are intended for intracranial vascular occlusion (permanent or temporary) of small vessels. The Aesculap AVM Microclip Applier is intended for holding and applying intracranial AVM Microclips.

Source page: https://510kreport.com/device/K024349
Methodology: https://510kreport.com/methodology