Cleared Traditional

K182580 - Novidia Flowable Composite (FDA 510(k) Clearance)

Jul 2019
Decision
287d
Days
Class 2
Risk

K182580 is an FDA 510(k) clearance for the Novidia Flowable Composite. This device is classified as a Material, Tooth Shade, Resin (Class II - Special Controls, product code EBF).

Submitted by Nobio , Ltd. (Petach Tikva, IL). The FDA issued a Cleared decision on July 3, 2019, 287 days after receiving the submission on September 19, 2018.

This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3690.

Submission Details

510(k) Number K182580 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 19, 2018
Decision Date July 03, 2019
Days to Decision 287 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF

Device Classification

Product Code EBF - Material, Tooth Shade, Resin
Device Class Class II - Special Controls
CFR Regulation 21 CFR 872.3690