# K233552: IDEAL Ziploop

- Pathway: 510(k) (Special)
- Applicant: Riverpoint Medical
- Decided: Nov 30, 2023 after 27 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). 60 ancestors in all.
No later device cites it as a predicate yet.
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 5.
- K230212: OrthoButton AL, Riverpoint Medical, LLC (2023) Summary page 5.

## Indications for use
The Riverpoint Medical IDEAL Ziploop 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/K233552
Methodology: https://510kreport.com/methodology