# K083161: Zen Wireless Footswitch (W1000), Zen Wireless Footswitch Adapter (W1100)

- Pathway: 510(k) (Traditional)
- Applicant: Conmed Linvatec
- Decided: Mar 27, 2009 after 151 days
- Product code: HRX (Arthroscope)
- Device class: 2
- Regulation: 21 CFR 888.1100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K931783 (1993). 39 ancestors in all.
9 later devices descend from it; 1 cites it directly.
0 of 49 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K990524: E9000 System, Linvatec Corp. (1999) Summary page 1.
- K033135: Stryker Wireless Universal Footswitch System, Stryker Endoscopy (2004) Summary page 1.
- K053510: IR Wireless Foot Switch, Linemaster Switch Corp. (2006) Summary page 1.

## Most influential descendants
- K100638: Vapr Vue Radiofrequency System ,Model 225024, VPR Vue Wireless Footswitch, Model 227214 (2010), 8 descendants of its own
- K152777: Bovie Disposable Bipolar Ablator (2016), 3 descendants of its own
- K161558: Bovie 3.3mm Disposable Bipolar Ablator 90°, Aspirating and Non-Aspirating, Bovie 2.4mm Disposable Bipolar Ablator 55°, Non-Aspirating,  Bovie 1.8mm Disposable Bipolar Ablator 60°, Non-Aspirating (2016), 2 descendants of its own
- K231126: Eblator Device (2023), 1 descendant of its own
- K251899: E Blator (2025), 0 descendants of its own

## Indications for use
The ConMed Linvatec Zen TM Wireless Footswitch and Adapter is an accessory that is intended to interface with compatible ConMed Linvatec power drive consoles to selectively control ConMed Linvatec surgical instruments.

Source page: https://510kreport.com/device/K083161
Methodology: https://510kreport.com/methodology