# K993575: Resolve Quickanchor

- Pathway: 510(k) (Traditional)
- Applicant: Mitek Products
- Decided: Dec 29, 1999 after 69 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: 2 generations back to K915889 (1992). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K970896: Mitek 3.5 MM Panalok Wedge Absorbable Suture Anchor System, ETHICON, Inc. (1997) Summary page 1.
- K962511: Mitek Micro Anchor, Mitek Products (1996) Summary page 1.
- K982420: Mitek Micro Anchor, Mitek Products (1998) Summary page 1.
- K992611: Mitek Rotator Cuff Quickanchor Plus, Mitek Products (1999) Summary page 1.

## Indications for use
The ReSolve™ QuickAnchor is used for the fixation of absorbable monofilament polydioxanone surgical suture to bone. This product is intended for the following indications: Cranio/Maxillofacial: Repair, reconstruction or reattachment of tendons, ligaments, muscles and soft tissue flaps to the parietal, temporal ridge, frontal, mandible, maxilla, zygoma and periorbital bones of the skull.

Source page: https://510kreport.com/device/K993575
Methodology: https://510kreport.com/methodology