# K014037: SJM Seguin Annuloplasty Ring (Seguin Ring), Model Sarp-(Size)

- Pathway: 510(k) (Special)
- Applicant: St. Jude Medical, Inc.
- Decided: Jan 4, 2002 after 28 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: 1 generation back to K961246 (1997). 1 ancestor in all.
2 later devices descend 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)
- K961246: SJM Seguin Annuloplasty Ring Model Sar-M, St. Jude Medical, Inc. (1997) Summary page 2.
- (no number) Seguin ring model SAR: named in the summary without a submission number

## Most influential descendants
- K092310: Seguin Annuloplasty Ring (2009), 1 descendant of its own
- 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 a mitral valve that is diseased or damaged due to acquired or congenital processes.

Source page: https://510kreport.com/device/K014037
Methodology: https://510kreport.com/methodology