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FDA 510(k)

ACE VERSANAIL

K-Number: K023115 · 2002-12-18

ApplicantDePuy Orthopaedics, Inc.
Decision Date2002-12-18
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACE VERSANAIL is the device name listed in this FDA 510(k) record. The listed applicant is DePuy Orthopaedics, Inc.. It received FDA 510(k) clearance on 2002-12-18 under 510(k) number K023115. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACE VERSANAIL?

ACE VERSANAIL is a medical device that received FDA 510(k) clearance on 2002-12-18. The listed applicant is DePuy Orthopaedics, Inc.. The 510(k) number is K023115.

When did ACE VERSANAIL receive FDA 510(k) clearance?

ACE VERSANAIL received FDA 510(k) clearance on 2002-12-18, under 510(k) number K023115.

Who is the listed applicant for ACE VERSANAIL?

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

What is the FDA product code for ACE VERSANAIL?

The FDA product code for ACE VERSANAIL is HSB.

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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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