RecallHawk

Asnis III Cannulated Screw System, Asnis PRO Cannulated Screw System

Stryker GmbH

Summary

Stryker GmbH received 510(k) clearance for Asnis III Cannulated Screw System, Asnis PRO Cannulated Screw System, a HWC device. Cleared on 2022-06-10.

Details

Source

510(k) Clearance

External ID

K220319

Action Date

2022-06-10

Status

Traditional

Category

device

Product Code

HWC

Product Description

Asnis III Cannulated Screw System, Asnis PRO Cannulated Screw System. Product code: HWC.

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. Stryker GmbH has received 17 total clearances in our database.

Stryker GmbH has 27 FDA actions in our database, including 10 recalls and 17 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 Stryker GmbH have FDA actions?

Stryker GmbH has 27 FDA actions in our database, including 10 recalls and 17 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K220319" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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