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GEISTLICH BIO-OSS PEN (0.25 G, 0.25-1.0MM GRANULES), GEISTLICH BIO-OSS PEN (0.5 G, 0.25-1.0MM GRANULES), GEISTLICH BIO-O

K120601 Class II Traditional
Decision Date
2012-05-24
Sponsor / Applicant
Geistlich Pharma AG

Technical Specification

510(k) Submission ID K120601
Product Code NPM
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3930
Decision Date 2012-05-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GEISTLICH BIO-OSS PEN (0.25 G, 0.25-1.0MM GRANULES), GEISTLICH BIO-OSS PEN (0.5 G, 0.25-1.0MM GRANULES), GEISTLICH BIO-O received FDA 510(k) clearance under submission number K120601, sponsored by Geistlich Pharma AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2012-05-24.

Classification & Regulation

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