# K060414: Kolster Methods, Inc., Featherlift Silhouette Suture

- Pathway: 510(k) (Traditional)
- Applicant: Kmi Kolster Methods, Inc.
- Decided: Oct 23, 2006 after 249 days
- Product code: GAW (Suture, Nonabsorbable, Synthetic, Polypropylene)
- Device class: 2
- Regulation: 21 CFR 878.5010
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K171005: Silhouette Featherlift (2017), 1 descendant of its own
- K191299: Silhouette Featherlift / Silhouette Lift (2019), 0 descendants of its own

## Recalls of this device
- Jul 2, 2015 · Class II · Z-2208-2015: Silhouette Lift is recalling the Silhouette Suture brochure because it does not include a complete list of risks and side effects. Therefore, it can potentially mislead the patient regarding the safet

## Indications for use
The Featherlift silhouette Suture is indicated for use in mid-face suspension surgery to fixate the cheek sub dermis in an elevated position.

Source page: https://510kreport.com/device/K060414
Methodology: https://510kreport.com/methodology