# K041159: JMS Absorbable Anchor and Applicator

- Pathway: 510(k) (Traditional)
- Applicant: Jms, Inc.
- Decided: Jul 27, 2004 after 85 days
- Product code: GDW (Staple, Implantable)
- Device class: 2
- Regulation: 21 CFR 878.4750
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Absorbable AnchorTM and Applicator are indicated for fixation of prosthetic material to soft tissue in various minimally invasive and open general surgical procedures, such as hernia repair.

Source page: https://510kreport.com/device/K041159
Methodology: https://510kreport.com/methodology