Cleared Traditional

K213209 - EZ-TRAX Zimmer G7 Acetabular System / Taperloc Complete Hip System Containment Device (FDA 510(k) Clearance)

Dec 2021
Decision
90d
Days
Class 2
Risk

K213209 is an FDA 510(k) clearance for the EZ-TRAX Zimmer G7 Acetabular System / Taperloc Complete Hip System Containment Device. This device is classified as a Sterilization Wrap Containers, Trays, Cassettes & Other Accessories (Class II - Special Controls, product code KCT).

Submitted by K1 Medical, LLC (Woodbridge, US). The FDA issued a Cleared decision on December 28, 2021, 90 days after receiving the submission on September 29, 2021.

This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 880.6850.

Submission Details

510(k) Number K213209 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 29, 2021
Decision Date December 28, 2021
Days to Decision 90 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF

Device Classification

Product Code KCT — Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Device Class Class II - Special Controls
CFR Regulation 21 CFR 880.6850

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