# K024115: Microfix Quickanchor Plus

- Pathway: 510(k) (Traditional)
- Applicant: Mitek Worldwide
- Decided: Mar 13, 2003 after 90 days
- Product code: HWC (Screw, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 1 cites it directly.
0 of 6 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) MICRO Anchor: named in the summary without a submission number
- (no number) Resolve QuickAnchor: named in the summary without a submission number
- (no number) BIOFASTIN RC suture anchors: named in the summary without a submission number

## Most influential descendants
- K080352: Micro QA+ Anchor Witht #3-0 Orthocord Suture, Model 212843, Microfix AQ+ Anchor with #3-0 Orthocord Suture (2008), 4 descendants of its own
- K110879: Biomet Sports Medicine Juggerknot (TM) Mini Soft Anchor (2011), 2 descendants of its own
- K254229: Arthrex Nano FiberTak Suture Anchor (2026), 0 descendants of its own
- K140908: Juggerknot Mini Soft Anchor (2014), 0 descendants of its own
- K123668: Orthocord (2013), 0 descendants of its own

## Indications for use
The MICROFIX QUICKANCHOR Plus is intended for fixation of soft tissue to bone, using suture, for the indications listed below: Hand: Repair/reconstruction of collateral ligaments, flexor and extensor tendon at the PIP (proximal interphalangeal), DIP (distal interphalangeal) and MCP (metacarpal interphalangeal) joints for all digits. Skull: Soft tissue attachment to the parietal, temporal ridge, frontal, mandible, maxilla, zygoma, and periorbital bones of the skull.

Source page: https://510kreport.com/device/K024115
Methodology: https://510kreport.com/methodology