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NobelSpeedy Groovy

K160119 Class II Traditional
Decision Date
2016-06-02
Sponsor / Applicant
Nobel Biocare AB

Technical Specification

510(k) Submission ID K160119
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2016-06-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NobelSpeedy Groovy received FDA 510(k) clearance under submission number K160119, sponsored by Nobel Biocare AB. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2016-06-02.

Classification & Regulation

This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.