meddevicedb.com FDA Device Reference

FLOWER SMALL AND MEDIUM IMPLANT SET

K131657 Class II Special
Decision Date
2013-08-22
Sponsor / Applicant
Flower Orthopedics Corporation

Technical Specification

510(k) Submission ID K131657
Product Code HRS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2013-08-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLOWER SMALL AND MEDIUM IMPLANT SET received FDA 510(k) clearance under submission number K131657, sponsored by Flower Orthopedics Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2013-08-22.

Classification & Regulation

This clearance is catalogued under FDA product code HRS and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.