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REFLECTION ACETABULAR REINFORCEMENT RINGS

K962541 Class II Traditional
Decision Date
1996-09-17
Sponsor / Applicant
Smith & Nephew Richards, Inc.

Technical Specification

510(k) Submission ID K962541
Product Code JDJ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 1996-09-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REFLECTION ACETABULAR REINFORCEMENT RINGS received FDA 510(k) clearance under submission number K962541, sponsored by Smith & Nephew Richards, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1996-09-17.

Classification & Regulation

This clearance is catalogued under FDA product code JDJ and 21 CFR 878.3300, within the General, Plastic Surgery review panel as a Class II device.