meddevicedb.com FDA Device Reference

IBS-B MIS Beveled Screw System

K231236 Class II Traditional
Decision Date
2023-07-27
Sponsor / Applicant
In2bones USA, LLC

Technical Specification

510(k) Submission ID K231236
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2023-07-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IBS-B MIS Beveled Screw System received FDA 510(k) clearance under submission number K231236, sponsored by In2bones USA, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2023-07-27.

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.