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FDA 510(k)

Logical Liner; World Liner; World Knee Patella

K-Number: K241690 · 2024-08-01

ApplicantSignature Orthopaedics Pty, Ltd.
Decision Date2024-08-01
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Logical Liner; World Liner; World Knee Patella is the device name listed in this FDA 510(k) record. The listed applicant is Signature Orthopaedics Pty, Ltd.. It received FDA 510(k) clearance on 2024-08-01 under 510(k) 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. The listed applicant is Signature Orthopaedics Pty, Ltd.. The 510(k) number is K241690.

When did Logical Liner; World Liner; World Knee Patella receive FDA 510(k) clearance?

Logical Liner; World Liner; World Knee Patella received FDA 510(k) clearance on 2024-08-01, under 510(k) number K241690.

Who is the listed applicant for Logical Liner; World Liner; World Knee Patella?

The FDA 510(k) record lists Signature Orthopaedics Pty, Ltd. as the applicant. This does not by itself establish the device manufacturer.

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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