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FDA 510(k)

STRYKER PLATING SYSTEM PERIARTICULAR PLATES

K-Number: K031959 · 2003-07-25

ApplicantHowmedica Osteonics Corp.
Decision Date2003-07-25
Product CodeLXT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

STRYKER PLATING SYSTEM PERIARTICULAR PLATES is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Osteonics Corp.. It received FDA 510(k) clearance on 2003-07-25 under 510(k) number K031959. The device is classified under product code LXT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER PLATING SYSTEM PERIARTICULAR PLATES?

STRYKER PLATING SYSTEM PERIARTICULAR PLATES is a medical device that received FDA 510(k) clearance on 2003-07-25. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K031959.

When did STRYKER PLATING SYSTEM PERIARTICULAR PLATES receive FDA 510(k) clearance?

STRYKER PLATING SYSTEM PERIARTICULAR PLATES received FDA 510(k) clearance on 2003-07-25, under 510(k) number K031959.

Who is the listed applicant for STRYKER PLATING SYSTEM PERIARTICULAR PLATES?

The FDA 510(k) record lists Howmedica Osteonics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STRYKER PLATING SYSTEM PERIARTICULAR PLATES?

The FDA product code for STRYKER PLATING SYSTEM PERIARTICULAR PLATES is LXT.

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Related Devices (Code: LXT)

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.

K230067Para-Fix External Fixation SystemNew Paradigm BiomedicalK131636POLARUS CONNECTAcumed, LLCK132704DISTAL RADIUS VOLAR RIM PLATE STANDARD, DISTAL RADIUS VOLAR RIM PLATE NARROWBiometK112345DISTAL VOLAR RADIUS PLATING SYSTEMSMedos International SARLK090374STERILE DVR ANATOMIC PLATES VARIOUS CONFIGURATIONS) MODEL (S) 131212001,2, 5-10 2.5MM THREADED AND SMOOTH PEGS, MODEL(SDePuy Orthopaedics, Inc.K073135SYNTHES (USA) HYBRID EXTERNAL FIXATOR MODIFICATIONSSynthes (Usa)

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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