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FDA 510(k)

LPS UPPER EXTREMITY

K-Number: K042664 · 2004-12-08

ApplicantDepuy, Inc.
Decision Date2004-12-08
Product CodeJDC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LPS UPPER EXTREMITY is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 2004-12-08 under 510(k) number K042664. The device is classified under product code JDC. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LPS UPPER EXTREMITY?

LPS UPPER EXTREMITY is a medical device that received FDA 510(k) clearance on 2004-12-08. The listed applicant is Depuy, Inc.. The 510(k) number is K042664.

When did LPS UPPER EXTREMITY receive FDA 510(k) clearance?

LPS UPPER EXTREMITY received FDA 510(k) clearance on 2004-12-08, under 510(k) number K042664.

Who is the listed applicant for LPS UPPER EXTREMITY?

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

What is the FDA product code for LPS UPPER EXTREMITY?

The FDA product code for LPS UPPER EXTREMITY is JDC.

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Other records listing Depuy, Inc. as applicant

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.

K043058PINNACLE CONSTRAINED ACETABULAR LINERSK041085LPS (LIMB PRESERVATION SYSTEM) LOWER EXTREMITY DOVETAIL INTERCALARYK033959LPSK040544DURALOC OPTION ACETABULAR CUP SYSTEM, MODELS 1599-01-044 TO -066, 1599-11-044 TO -062 AND 1599-21-044 TO -062K021478DELTA SHOULDERK033329DEPUY ACE UNIVERSAL AND TROCH ENTRY FEMORAL NAIL SYSTEMS

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Related Devices (Code: JDC)

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.

K181362TEMA Elbow SystemLima Corporate S.P.A.K181307Zimmer Nexel Total Elbow, Connrad/Morrey Total ElbowZimmer, Inc.K153398Comprehensive SRS/Nexel ElbowBiomet Manufacturing CorpK123862ZIMMER NEXEL TOTAL ELBOWZimmer, Inc.K090473DISCOVERY ELBOW - X-SMALLBiomet Manufacturing CorpK060696ACCLAIM TOTAL ELBOW SYSTEMDePuy Orthopaedics, Inc.

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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