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BIO-BLOCKS

K970569 Class II Traditional
Decision Date
2000-08-14
Sponsor / Applicant
Geistlich-Pharma

Technical Specification

510(k) Submission ID K970569
Product Code LYC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3930
Decision Date 2000-08-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIO-BLOCKS received FDA 510(k) clearance under submission number K970569, sponsored by Geistlich-Pharma. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2000-08-14.

Classification & Regulation

This clearance is catalogued under FDA product code LYC and 21 CFR 872.3930, within the Dental review panel as a Class II device.