# K913450: Heart Technology Rotablator Wireclip

- Pathway: 510(k) (Traditional)
- Applicant: Heart Technology, Inc.
- Decided: Sep 6, 1991 after 35 days
- Product code: MCW (Catheter, Peripheral, Atherectomy)
- Device class: 2
- Regulation: 21 CFR 870.4875
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K121774: Rotablator Rotational Atherectomy System with Peripheral Rotalink Plus (2012), 2 descendants of its own
- K133566: Rotablator Rotational Atherectomy System with the Peripheral Rotalink Plus (2013), 1 descendant of its own
- K220962: ROTAPRO Rotational Atherectomy System (2022), 0 descendants of its own

Source page: https://510kreport.com/device/K913450
Methodology: https://510kreport.com/methodology