meddevicedb.com FDA Device Reference

SGARLATO LESSER TOE IMPLANT

K884739 Class II Traditional
Decision Date
1989-05-18
Sponsor / Applicant
Sgarlato Laboratories, Inc.

Technical Specification

510(k) Submission ID K884739
Product Code KWH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3720
Decision Date 1989-05-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SGARLATO LESSER TOE IMPLANT received FDA 510(k) clearance under submission number K884739, sponsored by Sgarlato Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1989-05-18.

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.