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FDA 510(k)

MODIFICATION TO VKS KNEE SYSTEM

K-Number: K023416 · 2002-11-08

ApplicantPlus Orthopedics
Decision Date2002-11-08
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO VKS KNEE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Plus Orthopedics. It received FDA 510(k) clearance on 2002-11-08 under 510(k) number K023416. 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 MODIFICATION TO VKS KNEE SYSTEM?

MODIFICATION TO VKS KNEE SYSTEM is a medical device that received FDA 510(k) clearance on 2002-11-08. The listed applicant is Plus Orthopedics. The 510(k) number is K023416.

When did MODIFICATION TO VKS KNEE SYSTEM receive FDA 510(k) clearance?

MODIFICATION TO VKS KNEE SYSTEM received FDA 510(k) clearance on 2002-11-08, under 510(k) number K023416.

Who is the listed applicant for MODIFICATION TO VKS KNEE SYSTEM?

The FDA 510(k) record lists Plus Orthopedics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFICATION TO VKS KNEE SYSTEM?

The FDA product code for MODIFICATION TO VKS KNEE SYSTEM is JWH.

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Other records listing Plus Orthopedics as applicant

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.

K032126PROMOS SHOULDERK033763MODIFICATION TO SLIM GLIDING NAIL SYSTEMK032709MODULAR PLUS HIP STEMK032548IP-XS COMPRESSION NAIL SYSTEMK032215VKS/TC-PLUS REVISION KNEEK032052UC-PLUS SOLUTION UNICONDYLAR KNEE

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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.

K262057GMK ExtensionMedacta International SAK260063GSPE SpacerThe General Hospital Corporation, d/b/a MassachusettsK262293EVOLUTION MPX™ Total Knee SystemSuzhou Microport Orthorecon Co., Ltd.K262341b-ONE® Mobio™ Total Knee System Revision Cemented Tibial Augments, Stem Extensions and Press-Fit Stem ExtensionsB-One Ortho, Corp.K262130ATTUNE Revision Knee SystemDepuy Orthopaedics, Inc.K253961SK Knee SystemJust Medical Devices (Tianjin) Co., Ltd.

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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