meddevicedb.com FDA Device Reference

PIT’Stop® implant

K170688 Class II Traditional
Decision Date
2017-11-28
Sponsor / Applicant
In2bones Sas

Technical Specification

510(k) Submission ID K170688
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2017-11-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PIT’Stop® implant received FDA 510(k) clearance under submission number K170688, sponsored by In2bones Sas. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2017-11-28.

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.