# K014161: SJM Tailor Annuloplasty Ring Model Tarp- (Size)

- Pathway: 510(k) (Special)
- Applicant: St. Jude Medical, Inc.
- Decided: Jan 15, 2002 after 27 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 K000119 (2000). 1 ancestor in all.
3 later devices descend from it; 2 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K000119: SJM Tailor Annuloplasty Ring, Model Tarn, St. Jude Medical, Inc. (2000) Summary page 2.

## Most influential descendants
- K083835: Attune Adjustable Flexible Annuloplasty Ring Model Afr (2009), 1 descendant of its own
- K092876: SJM Attune Annuloplasty Ring (2009), 0 descendants of its own
- K022363: SJM Tailor Annuloplasty Band, Model Tab-(Size) (Tailor Band) (2002), 0 descendants of its own

## Indications for use
The SJM® Tailor™ annuloplasty ring is indicated for use in the repair of a mitral or tricuspid valve that is diseased or damaged due to acquired or congenital processes.

Source page: https://510kreport.com/device/K014161
Methodology: https://510kreport.com/methodology