RecallHawk

Affixus® Natural Nail® Proximal Humeral System

Zimmer Switzerland Manufacturing GmbH

Summary

Zimmer Switzerland Manufacturing GmbH received 510(k) clearance for Affixus® Natural Nail® Proximal Humeral System, a HSB device. Cleared on 2025-12-12.

Details

Source

510(k) Clearance

External ID

K253749

Action Date

2025-12-12

Status

Special

Category

device

Product Code

HSB

Product Description

Affixus® Natural Nail® Proximal Humeral System. Product code: HSB.

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. Zimmer Switzerland Manufacturing GmbH has received 4 total clearances in our database.

Zimmer Switzerland Manufacturing GmbH 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 Zimmer Switzerland Manufacturing GmbH have FDA actions?

Zimmer Switzerland Manufacturing GmbH 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 "K253749" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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