Cleared Traditional

K121846 - CONTIPLEX C CONTINUOUS PERIPHERAL NERVE BLOCK NEEDLE (FDA 510(k) Clearance)

Nov 2012
Decision
148d
Days
Class 2
Risk

K121846 is an FDA 510(k) clearance for the CONTIPLEX C CONTINUOUS PERIPHERAL NERVE BLOCK NEEDLE. This device is classified as a Needle, Conduction, Anesthetic (w/wo Introducer) (Class II - Special Controls, product code BSP).

Submitted by B.Braun Medical, Inc. (Allentown, US). The FDA issued a Cleared decision on November 20, 2012, 148 days after receiving the submission on June 25, 2012.

This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5150.

Submission Details

510(k) Number K121846 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 25, 2012
Decision Date November 20, 2012
Days to Decision 148 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF

Device Classification

Product Code BSP — Needle, Conduction, Anesthetic (w/wo Introducer)
Device Class Class II - Special Controls
CFR Regulation 21 CFR 868.5150

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