Alcantara Thoracolumbar Plate System
Summary
Camber Spine Technologies, LLC received 510(k) clearance for Alcantara Thoracolumbar Plate System, a KWQ device. Cleared on 2024-04-16.
Details
Source
510(k) Clearance
External ID
K232256
Action Date
2024-04-16
Status
Traditional
Category
device
Product Code
KWQ
Product Description
Alcantara Thoracolumbar Plate System. Product code: KWQ.
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. Camber Spine Technologies, LLC has received 2 total clearances in our database.
Camber Spine Technologies, LLC 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 Camber Spine Technologies, LLC have FDA actions?
Camber Spine Technologies, LLC 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 "K232256" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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