# K150824: TD-Wand

- Pathway: 510(k) (Traditional)
- Applicant: Tdm Surgitech, Inc.
- Decided: May 28, 2015 after 57 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K780977 (1978). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K960255: Ceramic Blade Electrode, Utah Medical Products, Inc. (1996) Summary page 4.
- (no number) Epitome: named in the summary without a submission number

## Indications for use
The TDM SurgiTech TD-Wand is intended for use in procedures that require precise cuts where only light or no hemostasis is desired using the cut mode and procedures where a greater level of hemostasis is desired using the coag and blend modes.

Source page: https://510kreport.com/device/K150824
Methodology: https://510kreport.com/methodology