meddevicedb.com FDA Device Reference

Palisades™ Buttress Plate System

K261309 Class II Traditional
Decision Date
2026-07-16
Sponsor / Applicant
Bethesda Medical Devices, LLC

Technical Specification

510(k) Submission ID K261309
Product Code KWQ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3060
Decision Date 2026-07-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Palisades™ Buttress Plate System received FDA 510(k) clearance under submission number K261309, sponsored by Bethesda Medical Devices, 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 2026-07-16.

Classification & Regulation

This clearance is catalogued under FDA product code KWQ and 21 CFR 888.3060, within the Orthopedic review panel as a Class II device.