meddevicedb.com FDA Device Reference

MICRO-SEAL ACETABULAR SYSTEM

K971718 Class II Traditional
Decision Date
1997-07-23
Sponsor / Applicant
Whiteside Biomechanics, Inc.

Technical Specification

510(k) Submission ID K971718
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 1997-07-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICRO-SEAL ACETABULAR SYSTEM received FDA 510(k) clearance under submission number K971718, sponsored by Whiteside Biomechanics, 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 1997-07-23.

Classification & Regulation

This clearance is catalogued under FDA product code LPH and 21 CFR 888.3358, within the Orthopedic review panel as a Class II device.