Cleared Traditional

K153595 - Optetrak Logic Metaphyseal Cones (FDA 510(k) Clearance)

Mar 2016
Decision
100d
Days
Class 2
Risk

K153595 is an FDA 510(k) clearance for the Optetrak Logic Metaphyseal Cones. This device is classified as a Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer (Class II - Special Controls, product code JWH).

Submitted by Exactech, Inc. (Gainesville, US). The FDA issued a Cleared decision on March 25, 2016, 100 days after receiving the submission on December 16, 2015.

This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3560.

Submission Details

510(k) Number K153595 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 16, 2015
Decision Date March 25, 2016
Days to Decision 100 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF

Device Classification

Product Code JWH — Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer
Device Class Class II - Special Controls
CFR Regulation 21 CFR 888.3560

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