meddevicedb.com FDA Device Reference

SmartRelease Endoscopic Soft Tissue Release System

K223406 Class II Traditional
Decision Date
2023-02-02
Sponsor / Applicant
Microaire Surgical Instruments

Technical Specification

510(k) Submission ID K223406
Product Code HRX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.1100
Decision Date 2023-02-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SmartRelease Endoscopic Soft Tissue Release System received FDA 510(k) clearance under submission number K223406, sponsored by Microaire Surgical Instruments. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2023-02-02.

Classification & Regulation

This clearance is catalogued under FDA product code HRX and 21 CFR 888.1100, within the Orthopedic review panel as a Class II device.