RecallHawk

VSP® Orthopedics System

3D Systems

Summary

3D Systems received 510(k) clearance for VSP® Orthopedics System, a PBF device. Cleared on 2021-11-10.

Details

Source

510(k) Clearance

External ID

K211244

Action Date

2021-11-10

Status

Traditional

Category

device

Product Code

PBF

Product Description

VSP® Orthopedics System. Product code: PBF.

Company

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. 3D Systems has received 2 total clearances in our database.

3D Systems 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 3D Systems have FDA actions?

3D Systems 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 "K211244" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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