RecallHawk

The Acumed Wrist Fixation System

Acumed, LLC

Summary

Acumed, LLC received 510(k) clearance for The Acumed Wrist Fixation System, a HRS device. Cleared on 2025-06-18.

Details

Source

510(k) Clearance

External ID

K251296

Action Date

2025-06-18

Status

Traditional

Category

device

Product Code

HRS

Product Description

The Acumed Wrist Fixation System. Product code: HRS.

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. Acumed, LLC has received 9 total clearances in our database.

Acumed, LLC has 17 FDA actions in our database, including 8 recalls and 9 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 Acumed, LLC have FDA actions?

Acumed, LLC has 17 FDA actions in our database, including 8 recalls and 9 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K251296" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for device

Related Actions