Cleared Traditional

K091566 - ZIMMER NATURAL NAIL SYSTEM CEPHALOMEDULLARY NAILS (FDA 510(k) Clearance)

Oct 2009
Decision
153d
Days
Class 2
Risk

K091566 is an FDA 510(k) clearance for the ZIMMER NATURAL NAIL SYSTEM CEPHALOMEDULLARY NAILS. This device is classified as a Rod, Fixation, Intramedullary And Accessories (Class II - Special Controls, product code HSB).

Submitted by Zimmer GmbH (Warsaw, US). The FDA issued a Cleared decision on October 28, 2009, 153 days after receiving the submission on May 28, 2009.

This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3020.

Submission Details

510(k) Number K091566 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 28, 2009
Decision Date October 28, 2009
Days to Decision 153 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF

Device Classification

Product Code HSB — Rod, Fixation, Intramedullary And Accessories
Device Class Class II - Special Controls
CFR Regulation 21 CFR 888.3020

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