# K061835: Stryker Silverglide Bipolar Forceps Reusable Cable; Disposable Cable

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Instruments
- Decided: Sep 8, 2006 after 71 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: 1 generation back to K042608 (2004). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K042608: Tecno Reusable Bipolar Cables, Model 190-100 and 190-110, Tecno Instruments (Pvt.), Ltd. (2004) Summary page 1.

## Cited in the summary but kept off the family tree
- K023996: Aloka SSD-3500 Ultrasound System, Aloka Co., Ltd. (2002). Our reading of the summary gave K023996, FDA’s number for Aloka SSD-3500 Ultrasound System (Aloka Co., Ltd.). Its FDA name has none of the distinctive words the summary uses for the device it names, “Modern Medical Equipment Mfg. Ltd. Disposable Bipolar Forceps Cable”. Kept off the family tree. Summary page 1.

## Indications for use
The Stryker Silverglide Bipolar Forceps Reusable Cable and Stryker Silverglide Bipolar Forceps Disposable Cable are intended to transfer electrosurgical power to bipolar forceps from an electrosurgical generator.

Source page: https://510kreport.com/device/K061835
Methodology: https://510kreport.com/methodology