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FDA 510(k)

DEPUY SUMMIT BASIC PRESS-FIT HIP STEM

K-Number: K030122 · 2003-02-05

ApplicantDePuy Orthopaedics, Inc.
Decision Date2003-02-05
Product CodeLWJ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DEPUY SUMMIT BASIC PRESS-FIT HIP 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 2003-02-05 under 510(k) number K030122. The device is classified under product code LWJ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEPUY SUMMIT BASIC PRESS-FIT HIP STEM?

DEPUY SUMMIT BASIC PRESS-FIT HIP STEM is a medical device that received FDA 510(k) clearance on 2003-02-05. The listed applicant is DePuy Orthopaedics, Inc.. The 510(k) number is K030122.

When did DEPUY SUMMIT BASIC PRESS-FIT HIP STEM receive FDA 510(k) clearance?

DEPUY SUMMIT BASIC PRESS-FIT HIP STEM received FDA 510(k) clearance on 2003-02-05, under 510(k) number K030122.

Who is the listed applicant for DEPUY SUMMIT BASIC PRESS-FIT HIP 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 SUMMIT BASIC PRESS-FIT HIP STEM?

The FDA product code for DEPUY SUMMIT BASIC PRESS-FIT HIP STEM is LWJ.

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Other records listing DePuy Orthopaedics, Inc. as applicant

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Related Devices (Code: LWJ)

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.

K120595UNISYN PLUS HIP STEMConsensus Orthopedics, Inc.K103518TRINITY ACETABULAR SYSTEMCorin USAK090764NOVATION CFS PRESS-FIT AND CEMENTED STEMSExactech, Inc.K082146METHA SHORT STEM HIP SYSTEM XL FEMORAL HEADAesculap Implant Systems, Inc.K07006136MM COCR FEMORAL HEAD AND 36MM ACETABULAR INSERTHayes Medical, Inc.K062978U2 HIP STEM, TI PLASMA SPRAYUnited Orthopedic Corp.

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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