# K113494: Noblestitch EL Noblestitch MR Noblestitch TA

- Pathway: 510(k) (Special)
- Applicant: Nobles Medical Technologies Ii, Inc.
- Decided: Apr 19, 2012 after 146 days
- Product code: GAW (Suture, Nonabsorbable, Synthetic, Polypropylene)
- Device class: 2
- Regulation: 21 CFR 878.5010
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) SuperStitch® Vascular Suturing Device: named in the summary without a submission number

## Most influential descendants
- K162617: NobleStitch EL (2017), 0 descendants of its own

## Indications for use
The NobleStitch EL, MR, and TA is indicated for use in performing vascular stitching in general surgery, including endoscopic procedures. The NobleStitch EL, MR, and TA is not intended for blind vascular closure.

Source page: https://510kreport.com/device/K113494
Methodology: https://510kreport.com/methodology
