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FDA 510(k)

NBX - NON-BRIDGING EXTERNAL FIXATOR

K-Number: K020905 · 2002-04-15

ApplicantBiomet Orthopedics, Inc.
Decision Date2002-04-15
Product CodeLXT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NBX - NON-BRIDGING EXTERNAL FIXATOR is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Orthopedics, Inc.. It received FDA 510(k) clearance on 2002-04-15 under 510(k) number K020905. 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 NBX - NON-BRIDGING EXTERNAL FIXATOR?

NBX - NON-BRIDGING EXTERNAL FIXATOR is a medical device that received FDA 510(k) clearance on 2002-04-15. The listed applicant is Biomet Orthopedics, Inc.. The 510(k) number is K020905.

When did NBX - NON-BRIDGING EXTERNAL FIXATOR receive FDA 510(k) clearance?

NBX - NON-BRIDGING EXTERNAL FIXATOR received FDA 510(k) clearance on 2002-04-15, under 510(k) number K020905.

Who is the listed applicant for NBX - NON-BRIDGING EXTERNAL FIXATOR?

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

What is the FDA product code for NBX - NON-BRIDGING EXTERNAL FIXATOR?

The FDA product code for NBX - NON-BRIDGING EXTERNAL FIXATOR is LXT.

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Other records listing Biomet Orthopedics, 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.

K253515Zimmer Biomet OSS™ Orthopedic Salvage System OsseoTi® Sleeves and AugmentsK080528E-POLY TIBIAL BEARINGSK072879INNERVUE DIAGNOSTIC SCOPE SYSTEMK070955ACID ETCHED LAG SCREWSK033355LACTOSCREW SCREW ANCHORK032286CALCIGEN PSI BONE GRAFT SUBSTITUTE

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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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