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FDA 510(k)

FOUNDATION MODULAR TIBIAL BASEPLATE

K-Number: K932425 · 1994-07-22

ApplicantEncore Orthopedics, Inc.
Decision Date1994-07-22
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

FOUNDATION MODULAR TIBIAL BASEPLATE is the device name listed in this FDA 510(k) record. The listed applicant is Encore Orthopedics, Inc.. It received FDA 510(k) clearance on 1994-07-22 under 510(k) number K932425. 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 FOUNDATION MODULAR TIBIAL BASEPLATE?

FOUNDATION MODULAR TIBIAL BASEPLATE is a medical device that received FDA 510(k) clearance on 1994-07-22. The listed applicant is Encore Orthopedics, Inc.. The 510(k) number is K932425.

When did FOUNDATION MODULAR TIBIAL BASEPLATE receive FDA 510(k) clearance?

FOUNDATION MODULAR TIBIAL BASEPLATE received FDA 510(k) clearance on 1994-07-22, under 510(k) number K932425.

Who is the listed applicant for FOUNDATION MODULAR TIBIAL BASEPLATE?

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

What is the FDA product code for FOUNDATION MODULAR TIBIAL BASEPLATE?

The FDA product code for FOUNDATION MODULAR TIBIAL BASEPLATE is JWH.

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Other records listing Encore Orthopedics, 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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