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FDA 510(k)

WHITESIDE ORTHOLOC M.A. TOTAL KNEE SYSTEM

K-Number: K893252 · 1989-07-28

ApplicantDow Corning Wright
Decision Date1989-07-28
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

WHITESIDE ORTHOLOC M.A. TOTAL KNEE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Dow Corning Wright. It received FDA 510(k) clearance on 1989-07-28 under 510(k) number K893252. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the WHITESIDE ORTHOLOC M.A. TOTAL KNEE SYSTEM?

WHITESIDE ORTHOLOC M.A. TOTAL KNEE SYSTEM is a medical device that received FDA 510(k) clearance on 1989-07-28. The listed applicant is Dow Corning Wright. The 510(k) number is K893252.

When did WHITESIDE ORTHOLOC M.A. TOTAL KNEE SYSTEM receive FDA 510(k) clearance?

WHITESIDE ORTHOLOC M.A. TOTAL KNEE SYSTEM received FDA 510(k) clearance on 1989-07-28, under 510(k) number K893252.

Who is the listed applicant for WHITESIDE ORTHOLOC M.A. TOTAL KNEE SYSTEM?

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

What is the FDA product code for WHITESIDE ORTHOLOC M.A. TOTAL KNEE SYSTEM?

The FDA product code for WHITESIDE ORTHOLOC M.A. TOTAL KNEE SYSTEM is JWH.

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Other records listing Dow Corning Wright 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.

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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