Cleared Traditional

K082560 - PANASIL IMPRESSION MATERIALS, INCLUDING PUTTY, BINETICS, TRAY, MONOPHASE AND CONTACT (FDA 510(k) Clearance)

Sep 2008
Decision
4d
Days
Class 2
Risk

K082560 is an FDA 510(k) clearance for the PANASIL IMPRESSION MATERIALS, INCLUDING PUTTY, BINETICS, TRAY, MONOPHASE AND CONTACT. This device is classified as a Material, Impression (Class II - Special Controls, product code ELW).

Submitted by Kettenbach GmbH & Co. KG (D-35713 Eschenburg, DE). The FDA issued a Cleared decision on September 8, 2008, 4 days after receiving the submission on September 4, 2008.

This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3660.

Submission Details

510(k) Number K082560 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 04, 2008
Decision Date September 08, 2008
Days to Decision 4 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF

Device Classification

Product Code ELW - Material, Impression
Device Class Class II - Special Controls
CFR Regulation 21 CFR 872.3660