RecallHawk

EZ-TRAX Zimmer G7 Acetabular System / Taperloc Complete Hip System Containment Device

K1 Medical, LLC

Summary

K1 Medical, LLC received 510(k) clearance for EZ-TRAX Zimmer G7 Acetabular System / Taperloc Complete Hip System Containment Device, a KCT device. Cleared on 2021-12-28.

Details

Source

510(k) Clearance

External ID

K213209

Action Date

2021-12-28

Status

Traditional

Category

device

Product Code

KCT

Product Description

EZ-TRAX Zimmer G7 Acetabular System / Taperloc Complete Hip System Containment Device. Product code: KCT.

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 413 device clearances issued this month.

Frequently Asked Questions

What does 510(k) clearance mean?

A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.

How often does K1 Medical, LLC have FDA actions?

This is the only FDA action we have on record for K1 Medical, LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K213209" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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