# K210675: EasyWhip

- Pathway: 510(k) (Traditional)
- Applicant: Winter Innovations, Inc.
- Decided: May 3, 2021 after 59 days
- Product code: GAT (Suture, Nonabsorbable, Synthetic, Polyethylene)
- Device class: 2
- Regulation: 21 CFR 878.5000
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K990088 (1999). 38 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 40 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K191268: Force Fiber Suture, Teleflex Medical Incorporated (2019) Summary page 4.

## Most influential descendants
- K261021: EasyWhip Family (2026), 0 descendants of its own

## Indications for use
EasyWhipm is indicated for use in approximation and/or ligation of soft tissues, including the use of allograft tissue for orthopedic surgeries.

Source page: https://510kreport.com/device/K210675
Methodology: https://510kreport.com/methodology