RecallHawk

MAGEC Spinal Bracing and Distraction System

Nuvasive Specialized Orthopedics, Incorporated

Summary

Nuvasive Specialized Orthopedics, Incorporated received 510(k) clearance for MAGEC Spinal Bracing and Distraction System, a PGN device. Cleared on 2024-02-06.

Details

Source

510(k) Clearance

External ID

K233593

Action Date

2024-02-06

Status

Traditional

Category

device

Product Code

PGN

Product Description

MAGEC Spinal Bracing and Distraction System. Product code: PGN.

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. Nuvasive Specialized Orthopedics, Incorporated has received 2 total clearances in our database.

Nuvasive Specialized Orthopedics, Incorporated 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 Nuvasive Specialized Orthopedics, Incorporated have FDA actions?

Nuvasive Specialized Orthopedics, Incorporated 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 "K233593" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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