# K992487: Mitek Mini Quickanchor Plus

- Pathway: 510(k) (Traditional)
- Applicant: Mitek Products
- Decided: Sep 21, 1999 after 57 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
Longest line of descent: 1 generation back to K921873 (1992). 3 ancestors in all.
67 later devices descend from it; 8 cite it directly.
0 of 71 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K921873: Quickanchor, Modification, Mitek Surgical Products, Inc. (1992) Summary page 1.
- K930892: Mitek Mini Anchor, Modification, Mitek Surgical Products, Inc. (1994) Summary page 1.
- K936311: Mitek Mini Anchor, Mitek Surgical Products, Inc. (1995) Summary page 1.

## Most influential descendants
- K061349: Opus Labralock P Knotless Fixation Device (2006), 50 descendants of its own
- K070227: Opus Magnum PI Knotless Fixation Device (2007), 27 descendants of its own
- K090615: Opus Speedlock Knotless Fixation Device (2009), 18 descendants of its own
- K081893: Opus Magnum Speedscrew Knotless Fixation Device, Model OM-6500 (2008), 16 descendants of its own
- K100457: Opus Speedscrew System (2010), 15 descendants of its own

## Indications for use
The Mitek Mini QuickAnchor® Plus is indicated for: shoulder (Bankart repair) ankle (Mid-foot reconstruction) foot (Hallux valgus reconstruction) hand (Ulnar or lateral collateral ligament reconstruction) wrist (Scapholunate ligament reconstruction) pubis (For relief from Stress Urinary Incontinence due to urethral or bladder neck hypermobility with minimal or no cystocele).

Source page: https://510kreport.com/device/K992487
Methodology: https://510kreport.com/methodology