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NATURAL LOCK ACETABULAR COMPONENT

K830662 Class III Traditional
Decision Date
1983-04-11
Sponsor / Applicant
Advanced Biosearch Assn.

Technical Specification

510(k) Submission ID K830662
Product Code JDL
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3320
Decision Date 1983-04-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NATURAL LOCK ACETABULAR COMPONENT received FDA 510(k) clearance under submission number K830662, sponsored by Advanced Biosearch Assn.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1983-04-11.

Classification & Regulation

This clearance is catalogued under FDA product code JDL and 21 CFR 888.3320, within the Orthopedic review panel as a Class III device.