# K013024: Selectiva Guidewire

- Pathway: 510(k) (Traditional)
- Applicant: Neometrics, Inc.
- Decided: Dec 4, 2001 after 88 days
- Product code: DQX (Wire, Guide, Catheter)
- Device class: 2
- Regulation: 21 CFR 870.1330
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K011084 (2001). 1 ancestor in all.
15 later devices descend from it; 4 cite it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K011084: Mandrel Guidewire Assembly, Lake Region Mfg., Inc. (2001) Summary page 1.

## Most influential descendants
- K031652: Vascupuncture Picc Guidewire (2003), 12 descendants of its own
- K040786: Vascupuncture Picc Guidewire with Hydro-Silk Coating (2004), 11 descendants of its own
- K043398: Modification to Vascupuncture Picc Guidewire (2005), 10 descendants of its own
- K112631: Vsi Guidewire (2011), 7 descendants of its own
- K133114: Micropuncture Introducer Set (2014), 4 descendants of its own

## Indications for use
The NeoMetrics Selectiva™ Guidewire is intended to facilitate the placement of devices for diagnostic and interventional procedures. NOTE: These guidewires are not intended for PTCA use.

Source page: https://510kreport.com/device/K013024
Methodology: https://510kreport.com/methodology