meddevicedb.com FDA Device Reference

OsteoCoil™ Nitinol Compression System (Multiple Component PNs)

K233567 Class II Traditional
Decision Date
2024-11-22
Sponsor / Applicant
Flower Orthopedics Corporation Dba Conventus Flower Ortho

Technical Specification

510(k) Submission ID K233567
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2024-11-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OsteoCoil™ Nitinol Compression System (Multiple Component PNs) received FDA 510(k) clearance under submission number K233567, sponsored by Flower Orthopedics Corporation Dba Conventus Flower Ortho. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2024-11-22.

Classification & Regulation

This clearance is catalogued under FDA product code HWC and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.