# K260106: OsteoCoil™ GT Active Compression System

- Pathway: 510(k) (Traditional)
- Applicant: Flower Orthopedics Corporation DBA Conventus Flower Orthoped
- Decided: Aug 24, 2026 after 222 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: 9 generations back to K962823 (1996). 35 ancestors in all.
No later device cites it as a predicate yet.
0 of 36 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K233567: OsteoCoil™ Nitinol Compression System (Multiple Component PNs), Flower Orthopedics Corporation Dba Conventus Flower Ortho (2024) Summary page 6.

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

Source page: https://510kreport.com/device/K260106
Methodology: https://510kreport.com/methodology