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FDA 510(k)

ANTEROLATERAL AND MEDIAL LOCKING PLATING SYSTEM

K-Number: K072832 · 2007-12-14

ApplicantDePuy Orthopaedics, Inc.
Decision Date2007-12-14
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ANTEROLATERAL AND MEDIAL LOCKING PLATING SYSTEM 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 2007-12-14 under 510(k) number K072832. 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 ANTEROLATERAL AND MEDIAL LOCKING PLATING SYSTEM?

ANTEROLATERAL AND MEDIAL LOCKING PLATING SYSTEM is a medical device that received FDA 510(k) clearance on 2007-12-14. The listed applicant is DePuy Orthopaedics, Inc.. The 510(k) number is K072832.

When did ANTEROLATERAL AND MEDIAL LOCKING PLATING SYSTEM receive FDA 510(k) clearance?

ANTEROLATERAL AND MEDIAL LOCKING PLATING SYSTEM received FDA 510(k) clearance on 2007-12-14, under 510(k) number K072832.

Who is the listed applicant for ANTEROLATERAL AND MEDIAL LOCKING PLATING SYSTEM?

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 ANTEROLATERAL AND MEDIAL LOCKING PLATING SYSTEM?

The FDA product code for ANTEROLATERAL AND MEDIAL LOCKING PLATING SYSTEM is HRS.

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Other records listing DePuy Orthopaedics, 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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