meddevicedb.com FDA Device Reference

SUTTER HAMMERTOE JOINT PROSTHESIS

K943354 Class II Traditional
Decision Date
1995-06-12
Sponsor / Applicant
Sutter Corp.

Technical Specification

510(k) Submission ID K943354
Product Code KWH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3720
Decision Date 1995-06-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUTTER HAMMERTOE JOINT PROSTHESIS received FDA 510(k) clearance under submission number K943354, sponsored by Sutter Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1995-06-12.

Classification & Regulation

This clearance is catalogued under FDA product code KWH and 21 CFR 888.3720, within the Orthopedic review panel as a Class II device.