Logical Liner; World Liner; World Knee Patella
K-Number: K241690 · 2024-08-01
Device Summary
Frequently Asked Questions
What is the Logical Liner; World Liner; World Knee Patella?
Logical Liner; World Liner; World Knee Patella is a medical device that received FDA 510(k) clearance on 2024-08-01. It is manufactured by Signature Orthopaedics Pty, Ltd.. The 510(k) number is K241690.
When was Logical Liner; World Liner; World Knee Patella approved by the FDA?
Logical Liner; World Liner; World Knee Patella received FDA 510(k) clearance on 2024-08-01, under approval number K241690.
What company makes Logical Liner; World Liner; World Knee Patella?
Logical Liner; World Liner; World Knee Patella is manufactured by Signature Orthopaedics Pty, Ltd..
What is the FDA product code for Logical Liner; World Liner; World Knee Patella?
The FDA product code for Logical Liner; World Liner; World Knee Patella is MEH.
Other Devices by Signature Orthopaedics Pty, Ltd.
Related Devices (Code: MEH)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.