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FDA 510(k)

VKS/TC-PLUS REVISION KNEE

K-Number: K032215 · 2003-08-08

ApplicantPlus Orthopedics
Decision Date2003-08-08
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VKS/TC-PLUS REVISION KNEE is the device name listed in this FDA 510(k) record. The listed applicant is Plus Orthopedics. It received FDA 510(k) clearance on 2003-08-08 under 510(k) number K032215. 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 VKS/TC-PLUS REVISION KNEE?

VKS/TC-PLUS REVISION KNEE is a medical device that received FDA 510(k) clearance on 2003-08-08. The listed applicant is Plus Orthopedics. The 510(k) number is K032215.

When did VKS/TC-PLUS REVISION KNEE receive FDA 510(k) clearance?

VKS/TC-PLUS REVISION KNEE received FDA 510(k) clearance on 2003-08-08, under 510(k) number K032215.

Who is the listed applicant for VKS/TC-PLUS REVISION KNEE?

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 VKS/TC-PLUS REVISION KNEE?

The FDA product code for VKS/TC-PLUS REVISION KNEE 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 SYSTEMK032052UC-PLUS SOLUTION UNICONDYLAR KNEEK031165PLUS ORTHOPEDICS CEMENTED HIP STEM

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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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