RecallHawk

Fassier-Duval Telescoping IM System

Orthopediatrics Canada Ulc Dba Pega Medical

Summary

Orthopediatrics Canada Ulc Dba Pega Medical received 510(k) clearance for Fassier-Duval Telescoping IM System, a HSB device. Cleared on 2025-02-21.

Details

Source

510(k) Clearance

External ID

K241983

Action Date

2025-02-21

Status

Traditional

Category

device

Product Code

HSB

Product Description

Fassier-Duval Telescoping IM 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 389 device clearances issued this month.

Orthopediatrics Canada Ulc Dba Pega Medical has 2 FDA actions in our database, including 1 recall and 1 clearance.

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 Orthopediatrics Canada Ulc Dba Pega Medical have FDA actions?

Orthopediatrics Canada Ulc Dba Pega Medical has 2 FDA actions in our database, including 1 recall and 1 device clearance.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K241983" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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