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AND Medical Femoral Nail System (PFNA01); AND Medical Femoral Nail System (PFNA02)

Suzhou and Science & Technology Development Corp.

Summary

Suzhou and Science & Technology Development Corp. received 510(k) clearance for AND Medical Femoral Nail System (PFNA01); AND Medical Femoral Nail System (PFNA02), a HSB device. Cleared on 2026-06-18.

Details

Source

510(k) Clearance

External ID

K253080

Action Date

2026-06-18

Status

Traditional

Category

device

Product Code

HSB

Product Description

AND Medical Femoral Nail System (PFNA01); AND Medical Femoral Nail System (PFNA02). 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 413 device clearances issued this month.

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 Suzhou and Science & Technology Development Corp. have FDA actions?

This is the only FDA action we have on record for Suzhou and Science & Technology Development Corp. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K253080" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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