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FDA 510(k)

DEPUY MOTECH ANTERIOR COMPRESSION PLATE SYSTEM

K-Number: K962486 · 1996-12-27

ApplicantDepuy, Inc.
Decision Date1996-12-27
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

DEPUY MOTECH ANTERIOR COMPRESSION PLATE 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 1996-12-27 under 510(k) number K962486. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the DEPUY MOTECH ANTERIOR COMPRESSION PLATE SYSTEM?

DEPUY MOTECH ANTERIOR COMPRESSION PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 1996-12-27. The listed applicant is Depuy, Inc.. The 510(k) number is K962486.

When did DEPUY MOTECH ANTERIOR COMPRESSION PLATE SYSTEM receive FDA 510(k) clearance?

DEPUY MOTECH ANTERIOR COMPRESSION PLATE SYSTEM received FDA 510(k) clearance on 1996-12-27, under 510(k) number K962486.

Who is the listed applicant for DEPUY MOTECH ANTERIOR COMPRESSION PLATE 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 DEPUY MOTECH ANTERIOR COMPRESSION PLATE SYSTEM?

The FDA product code for DEPUY MOTECH ANTERIOR COMPRESSION PLATE SYSTEM is KWQ.

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Other records listing Depuy, Inc. as applicant

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Related Devices (Code: KWQ)

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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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