# K233567: OsteoCoil™ Nitinol Compression System (Multiple Component PNs)

- Pathway: 510(k) (Traditional)
- Applicant: Flower Orthopedics Corporation Dba Conventus Flower Ortho
- Decided: Nov 22, 2024 after 382 days
- Product code: HWC (Screw, Fixation, Bone)
- 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: 8 generations back to K962823 (1996). 34 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 36 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K203595: DynaFuse Fixation System, MedShape, Inc. (2022) Summary page 5.

## Most influential descendants
- K260106: OsteoCoil™ GT Active Compression System (2026), 0 descendants of its own

## Indications for use
The OsteoCoil™ Nitinol Compression System is indicated for use in bone reconstruction, osteotomy, arthrodesis, joint fusion, fracture repair, and fracture fixation of the small bones for wrist, hand, and foot.

Source page: https://510kreport.com/device/K233567
Methodology: https://510kreport.com/methodology