RecallHawk

Minimally Invasive Prostate Surgery Navigation System(Model:AmaKris SR1-A-2)

Augment Intelligent Medical System (China) Co., Ltd.

Summary

Augment Intelligent Medical System (China) Co., Ltd. received 510(k) clearance for Minimally Invasive Prostate Surgery Navigation System(Model:AmaKris SR1-A-2), a LLZ device. Cleared on 2025-09-11.

Details

Source

510(k) Clearance

External ID

K242314

Action Date

2025-09-11

Status

Traditional

Category

device

Product Code

LLZ

Product Description

Minimally Invasive Prostate Surgery Navigation System(Model:AmaKris SR1-A-2). Product code: LLZ.

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. Augment Intelligent Medical System (China) Co., Ltd. has received 2 total clearances in our database.

Augment Intelligent Medical System (China) Co., 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 Augment Intelligent Medical System (China) Co., Ltd. have FDA actions?

Augment Intelligent Medical System (China) Co., 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 "K242314" 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