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FDA 510(k)

DEPUY MODULAR M HEADS

K-Number: K060031 · 2006-01-31

ApplicantDePuy Orthopaedics, Inc.
Decision Date2006-01-31
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DEPUY MODULAR M HEADS 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 2006-01-31 under 510(k) number K060031. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEPUY MODULAR M HEADS?

DEPUY MODULAR M HEADS is a medical device that received FDA 510(k) clearance on 2006-01-31. The listed applicant is DePuy Orthopaedics, Inc.. The 510(k) number is K060031.

When did DEPUY MODULAR M HEADS receive FDA 510(k) clearance?

DEPUY MODULAR M HEADS received FDA 510(k) clearance on 2006-01-31, under 510(k) number K060031.

Who is the listed applicant for DEPUY MODULAR M HEADS?

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 MODULAR M HEADS?

The FDA product code for DEPUY MODULAR M HEADS is LPH.

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Other records listing DePuy Orthopaedics, Inc. as applicant

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Related Devices (Code: LPH)

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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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