# K202399: OrthoButton FL

- Pathway: 510(k) (Special)
- Applicant: Riverpoint Medical
- Decided: Sep 18, 2020 after 28 days
- Product code: MBI (Fastener, Fixation, Nondegradable, Soft Tissue)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 13 generations back to K792022 (1979). 59 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 61 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K171060: OrthoButton AL, Riverpoint Medical (2017) Summary page 4.

## Most influential descendants
- K240194: ProCinch, QuadCinch (2024), 0 descendants of its own

## Indications for use
The Riverpoint Medical OrthoButton FL™ is intended for use in the fixation of bone and soft tissue in orthopedic procedures requiring ligament or tendon reconstruction.

Source page: https://510kreport.com/device/K202399
Methodology: https://510kreport.com/methodology