RecallHawk

TriALTIS™ Spine System

Medos International SARL

Summary

Medos International SARL received 510(k) clearance for TriALTIS™ Spine System, a NKB device. Cleared on 2025-10-21.

Details

Source

510(k) Clearance

External ID

K253249

Action Date

2025-10-21

Status

Special

Category

device

Product Code

NKB

Product Description

TriALTIS™ Spine System. Product code: NKB.

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. Medos International SARL has received 21 total clearances in our database.

Medos International SARL has 22 FDA actions in our database, including 1 recall and 21 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 Medos International SARL have FDA actions?

Medos International SARL has 22 FDA actions in our database, including 1 recall and 21 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K253249" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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