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FDA 510(k)

KONSTRUCT PATELLAR COMPONENT

K-Number: K960856 · 1996-11-27

ApplicantBiomet, Inc.
Decision Date1996-11-27
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

KONSTRUCT PATELLAR COMPONENT is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 1996-11-27 under 510(k) number K960856. 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 KONSTRUCT PATELLAR COMPONENT?

KONSTRUCT PATELLAR COMPONENT is a medical device that received FDA 510(k) clearance on 1996-11-27. The listed applicant is Biomet, Inc.. The 510(k) number is K960856.

When did KONSTRUCT PATELLAR COMPONENT receive FDA 510(k) clearance?

KONSTRUCT PATELLAR COMPONENT received FDA 510(k) clearance on 1996-11-27, under 510(k) number K960856.

Who is the listed applicant for KONSTRUCT PATELLAR COMPONENT?

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

What is the FDA product code for KONSTRUCT PATELLAR COMPONENT?

The FDA product code for KONSTRUCT PATELLAR COMPONENT is JWH.

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Other records listing Biomet, Inc. 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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