# K072298: Biopro Memory Staple, Models 18062-18073

- Pathway: 510(k) (Traditional)
- Applicant: Biopro, Inc.
- Decided: Oct 29, 2007 after 73 days
- Product code: JDR (Staple, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K221947: Tyber Medical Staple Fixation System (various) (2022), 0 descendants of its own

## Indications for use
1. Hand and foot bone fragment and osteotomy fixation and joint arthrodesis of the hand and foot bones.

Source page: https://510kreport.com/device/K072298
Methodology: https://510kreport.com/methodology