# K092310: Seguin Annuloplasty Ring

- Pathway: 510(k) (Special)
- Applicant: St Jude Medical
- Decided: Aug 27, 2009 after 29 days
- Product code: KRH (Ring, Annuloplasty)
- Device class: 2
- Regulation: 21 CFR 870.3800
- 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 K961246 (1997). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K014037: SJM Seguin Annuloplasty Ring (Seguin Ring), Model Sarp-(Size), St. Jude Medical, Inc. (2002) Summary page 1.

## Most influential descendants
- K253232: Seguin Annuloplasty Ring (2025), 0 descendants of its own

## Indications for use
The SJM Seguin annuloplasty ring is indicated for use in the repair of mitral valves that are diseased or damaged due to acquired or congenital processes.

Source page: https://510kreport.com/device/K092310
Methodology: https://510kreport.com/methodology