# K992623: Mitek Mini Anchor

- Pathway: 510(k) (Traditional)
- Applicant: Mitek Products
- Decided: Nov 2, 1999 after 89 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: 1 generation back to K921873 (1992). 3 ancestors in all.
14 later devices descend from it; 3 cite it directly.
0 of 18 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
- K030995: Minilok Quickanchor Plus (2003), 12 descendants of its own
- K071257: Mini Quickanchor and Quickanchor Plus with Orthocord (2007), 8 descendants of its own
- K212381: VersaTap, VersaLat, DueLock, VersaTi, MiniTi (2021), 1 descendant of its own
- K201636: Hercules Suture Anchor System (2020), 1 descendant of its own
- K153585: Flip Button Suture Anchor (2016), 1 descendant of its own

## Indications for use
Shoulder: Bankart Repair Ankle: Midfoot Reconstructions Foot: Hallux Valgus Reconstruction Wrist: Scapholunate Ligament Reconstruction Hand: Ulnar or Lateral Collateral Ligament Reconstruction Pubis: Fixation in the pubis for bladder neck suspension to resolve stress urinary incontinence The Mitek Mini Anchor is also indicated for the repair, repositioning or reattachment of soft tissues, ligaments and tendons to the mandible for surgical stabilization of the TMJ articular disc.

Source page: https://510kreport.com/device/K992623
Methodology: https://510kreport.com/methodology