# K041117: Panalok RC Quickanchor Plus, Model 212130, 212730; Dual Suture Panalok RC Quickanchor Pllus, Models 212132, 212732

- Pathway: 510(k) (Special)
- Applicant: Depuy Mitek
- Decided: May 28, 2004 after 29 days
- Product code: JDR (Staple, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3030
- 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 K964013 (1997). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K964013: Mitek Absorbable Toggle Anchor, Mitek Products (1997) Summary page 2.

## Most influential descendants
- K063273: Panalok Quickanchor Plus, Panalok RC Quickanchor Plus Dual Suture, Panalok Anchor (2006), 0 descendants of its own

## Indications for use
The Panalok RC QuickAnchor Plus and Dual Suture Panalok RC QuickAnchor Plus are intended for fixation of USP size #2 suture to bone for the indication listed below. Shoulder: Rotator cuff repair.

Source page: https://510kreport.com/device/K041117
Methodology: https://510kreport.com/methodology