Cleared Traditional

K040267 - TRIATHLON CRUCIATE RETAINING (CR) TOTAL KNEE (FDA 510(k) Clearance)

May 2004
Decision
90d
Days
Class 2
Risk

K040267 is an FDA 510(k) clearance for the TRIATHLON CRUCIATE RETAINING (CR) TOTAL KNEE. This device is classified as a Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer (Class II - Special Controls, product code JWH).

Submitted by Howmedica Osteonics Corp. (Mahwah, US). The FDA issued a Cleared decision on May 5, 2004, 90 days after receiving the submission on February 5, 2004.

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

Submission Details

510(k) Number K040267 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 05, 2004
Decision Date May 05, 2004
Days to Decision 90 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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