# K930892: Mitek Mini Anchor, Modification

- Pathway: 510(k) (Traditional)
- Applicant: Mitek Surgical Products, Inc.
- Decided: Jan 7, 1994 after 339 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
No predicates in its family tree.
598 later devices descend from it; 9 cite it directly.
0 of 599 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K962397: Statak Soft Tissue Attachment Device (1996), 531 descendants of its own
- K973015: Multitak SS Suture System (1997), 393 descendants of its own
- K990156: Multitak SS Buttons (1999), 336 descendants of its own
- K033717: Transet Fracture Fixation System (2004), 309 descendants of its own
- K043248: Tightrope Syndesmosis Repair Kit, Titanium, Model AR-8920DS; Stainless Steel. Model AR-8921DS (2005), 306 descendants of its own

Source page: https://510kreport.com/device/K930892
Methodology: https://510kreport.com/methodology