# K132047: Lemills Valvulotome

- Pathway: 510(k) (Traditional)
- Applicant: LeMaitre Vascular, Inc.
- Decided: Nov 5, 2013 after 126 days
- Product code: MGZ (Valvulotome)
- Device class: 2
- Regulation: 21 CFR 870.4885
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices 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) Mills Valvulotome, Pre-amendment device: named in the summary without a submission number

## Most influential descendants
- K142660: Antegrade LeMills Valvulotome (2014), 0 descendants of its own

## Indications for use
The LeMills Valvulotomne is intended to cut venous valves.

Source page: https://510kreport.com/device/K132047
Methodology: https://510kreport.com/methodology