# K936311: Mitek Mini Anchor

- Pathway: 510(k) (Traditional)
- Applicant: Mitek Surgical Products, Inc.
- Decided: Oct 31, 1995 after 559 days
- Product code: MNV (Strip, Dialysate Ph Indicator)
- Device class: 2
- Regulation: 21 CFR 876.5820
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
69 later devices descend from it; 2 cite it directly.
0 of 70 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K992487: Mitek Mini Quickanchor Plus (1999), 67 descendants of its own
- 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

Source page: https://510kreport.com/device/K936311
Methodology: https://510kreport.com/methodology