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FDA 510(k)

LinkSymphoKnee System

K-Number: K202924 · 2021-05-13

ApplicantWaldemar Link GmbH & Co. KG
Decision Date2021-05-13
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LinkSymphoKnee System is the device name listed in this FDA 510(k) record. The listed applicant is Waldemar Link GmbH & Co. KG. It received FDA 510(k) clearance on 2021-05-13 under 510(k) number K202924. 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 LinkSymphoKnee System?

LinkSymphoKnee System is a medical device that received FDA 510(k) clearance on 2021-05-13. The listed applicant is Waldemar Link GmbH & Co. KG. The 510(k) number is K202924.

When did LinkSymphoKnee System receive FDA 510(k) clearance?

LinkSymphoKnee System received FDA 510(k) clearance on 2021-05-13, under 510(k) number K202924.

Who is the listed applicant for LinkSymphoKnee System?

The FDA 510(k) record lists Waldemar Link GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LinkSymphoKnee System?

The FDA product code for LinkSymphoKnee System is JWH.

Other records listing Waldemar Link GmbH & Co. KG as applicant

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Related Devices (Code: JWH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261563Freedom Total Knee System (E-Poly Tibial Liners)Maxx Orthopedics, Inc.K262251ACTIFY™ Total Knee System, ACTIFY™ 3D Total Knee System (ACTIFY MC Tibial Insert)Globus Medical, Inc.K261734Klassic Infection Spacer SystemTotal Joint Orthopedics, Inc.K261458ATTUNE Total Knee System; ATTUNE Cementless Knee SystemDePuy Ireland UCK261032NovoKnee (SteriKnee)NovoSourceK253793Materialise TKA Guide SystemMaterialise NV

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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