Cleared Traditional

K022651 - HOFFMANN 30 DEGREE PELVIC DOUBLE BALL JOINT (FDA 510(k) Clearance)

Oct 2002
Decision
69d
Days
Class 2
Risk

K022651 is an FDA 510(k) clearance for the HOFFMANN 30 DEGREE PELVIC DOUBLE BALL JOINT. This device is classified as a Appliance, Fixation, Nail/blade/plate Combination, Multiple Component, Metal Composite (Class II - Special Controls, product code LXT).

Submitted by Howmedica Osteonics Corp. (Allendale, US). The FDA issued a Cleared decision on October 17, 2002, 69 days after receiving the submission on August 9, 2002.

This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3030.

Submission Details

510(k) Number K022651 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 09, 2002
Decision Date October 17, 2002
Days to Decision 69 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF

Device Classification

Product Code LXT — Appliance, Fixation, Nail/blade/plate Combination, Multiple Component, Metal Composite
Device Class Class II - Special Controls
CFR Regulation 21 CFR 888.3030