RecallHawk

SCOUT MD Surgical Guidance System

Merit Medical System, Inc.

Summary

Merit Medical System, Inc. received 510(k) clearance for SCOUT MD Surgical Guidance System, a NEU device. Cleared on 2024-02-12.

Details

Source

510(k) Clearance

External ID

K231468

Action Date

2024-02-12

Status

Traditional

Category

device

Product Code

NEU

Product Description

SCOUT MD Surgical Guidance System. Product code: NEU.

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. Merit Medical System, Inc. has received 4 total clearances in our database.

Merit Medical System, Inc. has 4 FDA actions in our database, including 4 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 Merit Medical System, Inc. have FDA actions?

Merit Medical System, Inc. has 4 FDA actions in our database, including 0 recalls and 4 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K231468" 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