# K924724: Kinetik Great Toe System

- Pathway: 510(k) (Traditional)
- Applicant: Kinetikos Medical, Inc.
- Decided: Jan 5, 1994 after 471 days
- Product code: LZJ (Prosthesis, Toe (Metatarsophalangeal), Joint, Metal/Polymer, Semi-Constrained)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
10 later devices descend from it; 2 cite it directly.
0 of 11 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
- K072251: Merete Toemobile Anatomical Great Toe Resurfacing System (2008), 9 descendants of its own
- K102549: The Ascension Movement Great Toe System Total Arthroplasty (2010), 8 descendants of its own
- K132496: Arthrosurface Toemotion (2014), 7 descendants of its own
- K152454: HemiCAP MTP Resurfacing Hemi-Arthroplasty System (2016), 6 descendants of its own
- K190543: Cannulated Hemi Implant (2019), 5 descendants of its own

Source page: https://510kreport.com/device/K924724
Methodology: https://510kreport.com/methodology