OGmend® Implant Enhancement System
Summary
Woven Orthopedic Technologies received 510(k) clearance for OGmend® Implant Enhancement System, a QVI device. Cleared on 2023-10-26.
Details
Source
510(k) Clearance
External ID
K233223
Action Date
2023-10-26
Status
Special
Category
device
Product Code
QVI
Product Description
OGmend® Implant Enhancement System. Product code: QVI.
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. Woven Orthopedic Technologies has received 2 total clearances in our database.
Woven Orthopedic Technologies 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 Woven Orthopedic Technologies have FDA actions?
Woven Orthopedic Technologies 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 "K233223" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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