Cleared Traditional

K141585 - SMITH & NEPHEW DISPOSABLE FIN PUNCH (FDA 510(k) Clearance)

Aug 2014
Decision
69d
Days
Class 2
Risk

K141585 is an FDA 510(k) clearance for the SMITH & NEPHEW DISPOSABLE FIN PUNCH. This device is classified as a Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer (Class II - Special Controls, product code JWH).

Submitted by Smith & Nephew, Inc. (Cordova, US). The FDA issued a Cleared decision on August 21, 2014, 69 days after receiving the submission on June 13, 2014.

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

Submission Details

510(k) Number K141585 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 13, 2014
Decision Date August 21, 2014
Days to Decision 69 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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