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FDA 510(k)

DEPUY TRI-LOCK BONE PRESERVATION STEM

K-Number: K073570 · 2008-02-21

ApplicantDePuy Orthopaedics, Inc.
Decision Date2008-02-21
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DEPUY TRI-LOCK BONE PRESERVATION STEM 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 2008-02-21 under 510(k) number K073570. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEPUY TRI-LOCK BONE PRESERVATION STEM?

DEPUY TRI-LOCK BONE PRESERVATION STEM is a medical device that received FDA 510(k) clearance on 2008-02-21. The listed applicant is DePuy Orthopaedics, Inc.. The 510(k) number is K073570.

When did DEPUY TRI-LOCK BONE PRESERVATION STEM receive FDA 510(k) clearance?

DEPUY TRI-LOCK BONE PRESERVATION STEM received FDA 510(k) clearance on 2008-02-21, under 510(k) number K073570.

Who is the listed applicant for DEPUY TRI-LOCK BONE PRESERVATION STEM?

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 DEPUY TRI-LOCK BONE PRESERVATION STEM?

The FDA product code for DEPUY TRI-LOCK BONE PRESERVATION STEM is LZO.

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Other records listing DePuy Orthopaedics, Inc. as applicant

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Related Devices (Code: LZO)

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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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