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SPIRIT RIDGE SILICONE CARVING BLOCK

K952706 Class II Traditional
Decision Date
1995-08-28
Sponsor / Applicant
Spirit Ridge Technologies

Technical Specification

510(k) Submission ID K952706
Product Code FZE
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3680
Decision Date 1995-08-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPIRIT RIDGE SILICONE CARVING BLOCK received FDA 510(k) clearance under submission number K952706, sponsored by Spirit Ridge Technologies. 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 1995-08-28.

Classification & Regulation

This clearance is catalogued under FDA product code FZE and 21 CFR 878.3680, within the General, Plastic Surgery review panel as a Class II device.