RecallHawk

Summary

Kyocera Medical Technologies, Inc. received 510(k) clearance for Initia Knee System, a JWH device. Cleared on 2025-01-13.

Details

Source

510(k) Clearance

External ID

K243295

Action Date

2025-01-13

Status

Traditional

Category

device

Product Code

JWH

Product Description

Initia Knee System. Product code: JWH.

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Kyocera Medical Technologies, Inc. has received 10 total clearances in our database.

Kyocera Medical Technologies, Inc. has 10 FDA actions in our database, including 10 clearances.

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 Kyocera Medical Technologies, Inc. have FDA actions?

Kyocera Medical Technologies, Inc. has 10 FDA actions in our database, including 0 recalls and 10 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K243295" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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