RecallHawk

XACT Robotic System, ACE Model

Xact Robotics, Ltd.

Summary

Xact Robotics, Ltd. received 510(k) clearance for XACT Robotic System, ACE Model, a JAK device. Cleared on 2022-09-23.

Details

Source

510(k) Clearance

External ID

K213759

Action Date

2022-09-23

Status

Traditional

Category

device

Product Code

JAK

Product Description

XACT Robotic System, ACE Model. Product code: JAK.

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. Xact Robotics, Ltd. has received 2 total clearances in our database.

Xact Robotics, Ltd. has 2 FDA actions in our database, including 2 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 Xact Robotics, Ltd. have FDA actions?

Xact Robotics, Ltd. has 2 FDA actions in our database, including 0 recalls and 2 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K213759" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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