# K930893: Mitek Super Quickanchor, Modification

- Pathway: 510(k) (Traditional)
- Applicant: Mitek Surgical Products, Inc.
- Decided: Dec 8, 1993 after 313 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.
24 later devices descend from it; 2 cite it directly.
0 of 25 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
- K041116: Super Quickanchor Plus (2004), 23 descendants of its own
- K052631: Super Quickanchor Plus (with Orthocord Suture) (2005), 22 descendants of its own
- K082282: Healix TI Anchor (2008), 21 descendants of its own
- K102298: Transtend BR Anchor W/ Orthocord, Transtend TI Anchor W/Orthocord, Transtend Peek Anchor W/Orthocord, Healix Transtend (2011), 15 descendants of its own
- K211002: Grappler Suture Anchor System (2021), 6 descendants of its own

Source page: https://510kreport.com/device/K930893
Methodology: https://510kreport.com/methodology