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FDA 510(k)

DEPUY ACE CALCANEAL PERI-ARTICULAR PLATE

K-Number: K993465 · 2000-01-11

ApplicantDepuy, Inc.
Decision Date2000-01-11
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DEPUY ACE CALCANEAL PERI-ARTICULAR PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 2000-01-11 under 510(k) number K993465. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEPUY ACE CALCANEAL PERI-ARTICULAR PLATE?

DEPUY ACE CALCANEAL PERI-ARTICULAR PLATE is a medical device that received FDA 510(k) clearance on 2000-01-11. The listed applicant is Depuy, Inc.. The 510(k) number is K993465.

When did DEPUY ACE CALCANEAL PERI-ARTICULAR PLATE receive FDA 510(k) clearance?

DEPUY ACE CALCANEAL PERI-ARTICULAR PLATE received FDA 510(k) clearance on 2000-01-11, under 510(k) number K993465.

Who is the listed applicant for DEPUY ACE CALCANEAL PERI-ARTICULAR PLATE?

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 ACE CALCANEAL PERI-ARTICULAR PLATE?

The FDA product code for DEPUY ACE CALCANEAL PERI-ARTICULAR PLATE is HRS.

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Other records listing Depuy, Inc. as applicant

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Related Devices (Code: HRS)

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.

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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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