# K240194: ProCinch, QuadCinch

- Pathway: 510(k) (Special)
- Applicant: Riverpoint Medical
- Decided: Feb 21, 2024 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: 14 generations back to K792022 (1979). 61 ancestors in all.
No later device cites it as a predicate yet.
0 of 62 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K202399: OrthoButton FL, Riverpoint Medical (2020) Summary page 5.
- K171060: OrthoButton AL, Riverpoint Medical (2017) Summary page 7.
- K230212: OrthoButton AL, Riverpoint Medical, LLC (2023) Summary page 7.

## Indications for use
The ProCinch, QuadCinch Adjustable Loop Device 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/K240194
Methodology: https://510kreport.com/methodology