# K060528: Aesculap Trelon Nonabsorbable Multifilament Polyamide Surgical Suture

- Pathway: 510(k) (Special)
- Applicant: Aesculap, Inc.
- Decided: Mar 28, 2006 after 28 days
- Product code: GAR (Suture, Nonabsorbable, Synthetic, Polyamide)
- Device class: 2
- Regulation: 21 CFR 878.5020
- 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 K990090 (1999). 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)
- K990090: Dafilon Nonabsorbable Polyamide Surgical Suture, Aesculap, Inc. (1999) Summary page 1.

## Indications for use
Trelon® sutures are intended for use in general and soft tissue approximation and/or ligation including use in cardiovascular, ophthalmic, and neurological procedures.

Source page: https://510kreport.com/device/K060528
Methodology: https://510kreport.com/methodology