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SOLID DILICONE IMPLANTS, SDILICONE SPONGE IMPLANTS

K950806 Class II Traditional
Decision Date
1996-06-05
Sponsor / Applicant
Mira, Inc.

Technical Specification

510(k) Submission ID K950806
Product Code HQX
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.3340
Decision Date 1996-06-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SOLID DILICONE IMPLANTS, SDILICONE SPONGE IMPLANTS received FDA 510(k) clearance under submission number K950806, sponsored by Mira, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1996-06-05.

Classification & Regulation

This clearance is catalogued under FDA product code HQX and 21 CFR 886.3340, within the Ophthalmic review panel as a Class II device.