meddevicedb.com FDA Device Reference

DynaNail TTC Fusion System

K250628 Class II Traditional
Decision Date
2025-09-12
Sponsor / Applicant
MedShape, Inc.

Technical Specification

510(k) Submission ID K250628
Product Code HSB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3020
Decision Date 2025-09-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DynaNail TTC Fusion System received FDA 510(k) clearance under submission number K250628, sponsored by MedShape, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2025-09-12.

Classification & Regulation

This clearance is catalogued under FDA product code HSB and 21 CFR 888.3020, within the Orthopedic review panel as a Class II device.