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FDA 510(k)

ANATOMIC MODULAR KNEE (AMK) SYSTEM

K-Number: K864671 · 1987-02-06

ApplicantDepuy, Inc.
Decision Date1987-02-06
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

ANATOMIC MODULAR KNEE (AMK) SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1987-02-06 under 510(k) number K864671. 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 ANATOMIC MODULAR KNEE (AMK) SYSTEM?

ANATOMIC MODULAR KNEE (AMK) SYSTEM is a medical device that received FDA 510(k) clearance on 1987-02-06. The listed applicant is Depuy, Inc.. The 510(k) number is K864671.

When did ANATOMIC MODULAR KNEE (AMK) SYSTEM receive FDA 510(k) clearance?

ANATOMIC MODULAR KNEE (AMK) SYSTEM received FDA 510(k) clearance on 1987-02-06, under 510(k) number K864671.

Who is the listed applicant for ANATOMIC MODULAR KNEE (AMK) SYSTEM?

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

What is the FDA product code for ANATOMIC MODULAR KNEE (AMK) SYSTEM?

The FDA product code for ANATOMIC MODULAR KNEE (AMK) SYSTEM is JWH.

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Other records listing Depuy, 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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