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FDA 510(k)

Freedom® Medial Congruent Liner

K-Number: K243277 · 2024-11-19

ApplicantMaxx Orthopedics, Inc.
Decision Date2024-11-19
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Freedom® Medial Congruent Liner is a medical device manufactured by Maxx Orthopedics, Inc.. It received FDA 510(k) clearance on 2024-11-19 under approval number K243277. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Freedom® Medial Congruent Liner?

Freedom® Medial Congruent Liner is a medical device that received FDA 510(k) clearance on 2024-11-19. It is manufactured by Maxx Orthopedics, Inc.. The 510(k) number is K243277.

When was Freedom® Medial Congruent Liner approved by the FDA?

Freedom® Medial Congruent Liner received FDA 510(k) clearance on 2024-11-19, under approval number K243277.

What company makes Freedom® Medial Congruent Liner?

Freedom® Medial Congruent Liner is manufactured by Maxx Orthopedics, Inc..

What is the FDA product code for Freedom® Medial Congruent Liner?

The FDA product code for Freedom® Medial Congruent Liner is JWH.

Related Clinical Trials

NCT05391828 Persona MC vs PS RCT With ROSA RECRUITING NCT07286513 Persona SoluTion PPS Femur PMCF ENROLLING_BY_INVITATION

Other Devices by Maxx Orthopedics, Inc.

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View all 17 devices →

Related Devices (Code: JWH)

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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.

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