Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Logical Liner; World Liner; World Knee Patella

K-Number: K241690 · 2024-08-01

Decision Date2024-08-01
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Logical Liner; World Liner; World Knee Patella is a medical device manufactured by Signature Orthopaedics Pty, Ltd.. It received FDA 510(k) clearance on 2024-08-01 under approval number K241690. The device is classified under product code MEH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 42 devices →

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.