# K140908: Juggerknot Mini Soft Anchor

- Pathway: 510(k) (Traditional)
- Applicant: Biomet Sports Medicine
- Decided: Oct 2, 2014 after 176 days
- Product code: DZL (Screw, Fixation, Intraosseous)
- Device class: 2
- Regulation: 21 CFR 872.4880
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K962793 (1996). 12 ancestors in all.
No later device cites it as a predicate yet.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K992623: Mitek Mini Anchor, Mitek Products (1999) Summary page 4.
- K992487: Mitek Mini Quickanchor Plus, Mitek Products (1999) Summary page 4.
- K080352: Micro QA+ Anchor Witht #3-0 Orthocord Suture, Model 212843, Microfix AQ+ Anchor with #3-0 Orthocord Suture, Depuy Mitek, A Johnson & Johnson Company (2008) Summary page 4.
- K110879: Biomet Sports Medicine Juggerknot (TM) Mini Soft Anchor, Biomet Sports Medicine (2011) Summary page 4.

## Indications for use
The JuggerKnot™ Mini Soft Anchors are intended to be used for soft tissue to bone fixation with indications for use in: Maxillofacial For the repair, repositioning or reattachment of soft tissues, ligament and tendons to the mandible for surgical stabilization of the TMJ articular disc.

Source page: https://510kreport.com/device/K140908
Methodology: https://510kreport.com/methodology