# K993327: Talon Anchor Snap-Pak

- Pathway: 510(k) (Traditional)
- Applicant: Mitek Products
- Decided: Dec 16, 1999 after 73 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: 1 generation back to K931782 (1994). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K931782: Mitek Giii Anchor, Mitek Surgical Products, Inc. (1994) Summary page 1.
- K962511: Mitek Micro Anchor, Mitek Products (1996) Summary page 1.
- K982420: Mitek Micro Anchor, Mitek Products (1998) Summary page 1.

## Indications for use
The TALON™ Anchor Snap-Pak is used for the fixation of non-absorbable braided surgical suture to bone. This product is intended for the following indications: Cranio/Maxillofacial: Repair and reconstruction or reattachment of tendons and 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/K993327
Methodology: https://510kreport.com/methodology