# K041116: Super Quickanchor Plus

- Pathway: 510(k) (Special)
- Applicant: Depuy Mitek
- Decided: May 28, 2004 after 29 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
Longest line of descent: 1 generation back to K930893 (1993). 1 ancestor in all.
23 later devices descend from it; 1 cites 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)
- K930893: Mitek Super Quickanchor, Modification, Mitek Surgical Products, Inc. (1993). Our reading of the summary gave K980893, which is not a number in FDA’s lists. Corrected to the number one digit away whose FDA name carries the summary’s words for the device, “SuperAnchor QuickAnchor”. Summary page 2.

## Most influential descendants
- 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
- K103712: Gryphon Peek DS Anchor W/ Orthocord, Gryphon Peek Anchor W/ Orthocord (2011), 6 descendants of its own

## Indications for use
The Mitek Super QUICKANCHOR Anchor Plus is intended for fixation of USP size #2 through #5 suture to bone for the indications listed below. Shoulder: Rotator cuff repair; capsular repair; biceps repair; deltoid repair. Ankle: Achilles tendon repair/reconstruction. Knee: Extra capsular repairs; Reattachment of: medial collateral ligament, lateral collateral ligament, posterior oblique ligament or joint capsule to tibia and joint capsule closure to anterior proximal tibia; extra capsular reconstruction, ITB tenodesis; patellar ligament and tendon avulsions.

Source page: https://510kreport.com/device/K041116
Methodology: https://510kreport.com/methodology