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FDA 510(k)

MODULAR ROTATING HINGE KNEE CROSSOVER TIBIAL BEARING COMPONENTS

K-Number: K001548 · 2000-06-07

ApplicantHowmedica Osteonics Corp.
Decision Date2000-06-07
Product CodeKRO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODULAR ROTATING HINGE KNEE CROSSOVER TIBIAL BEARING COMPONENTS 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 2000-06-07 under 510(k) number K001548. The device is classified under product code KRO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODULAR ROTATING HINGE KNEE CROSSOVER TIBIAL BEARING COMPONENTS?

MODULAR ROTATING HINGE KNEE CROSSOVER TIBIAL BEARING COMPONENTS is a medical device that received FDA 510(k) clearance on 2000-06-07. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K001548.

When did MODULAR ROTATING HINGE KNEE CROSSOVER TIBIAL BEARING COMPONENTS receive FDA 510(k) clearance?

MODULAR ROTATING HINGE KNEE CROSSOVER TIBIAL BEARING COMPONENTS received FDA 510(k) clearance on 2000-06-07, under 510(k) number K001548.

Who is the listed applicant for MODULAR ROTATING HINGE KNEE CROSSOVER TIBIAL BEARING COMPONENTS?

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 MODULAR ROTATING HINGE KNEE CROSSOVER TIBIAL BEARING COMPONENTS?

The FDA product code for MODULAR ROTATING HINGE KNEE CROSSOVER TIBIAL BEARING COMPONENTS is KRO.

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Other records listing Howmedica Osteonics Corp. as applicant

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Related Devices (Code: KRO)

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.

K261898Triathlon® Knee System; Triathlon® Hinge Knee System; Scorpio® Total Knee SystemHowmedica Osteonics Corp. dba Stryker OrthopaedicsK252898Triathlon® Tritanium® Asymmetric Patella; Triathlon® Tritanium® Symmetric Patella; Triathlon® Symmetric Patella; Triathlon® Asymmetric Patella; Scorpio® Universal Dome Patella; Triathlon® Hinge BumperHowmedica Osteonics Corp., Dba Stryker OrthopaedicsK252303Stem Extension Line (USTAR II System)United Orthopedic CorporationK251665Triathlon® Hinge Knee SystemHowmedica Osteonics Corp., Dba Stryker OrthopaedicsK242871ATTUNE™ Revision Hinge KneeDepuy Ireland UCK240043EVOLUTION® Hinge Knee System;GUARDIAN™ limb Salvage System;DCW Modular Distal Femoral System;REPIPHYSIS™ Limb Salvage System;EVOLUTION® MP Total Knee System; EVOLUTION® MP Total Knee System; EVOLUTION® MP Adaptive CS Insert; EVOLUTION® MP Adaptive PS Tibial Insert; EVOLUTION® MP CS/CR Porous Femur/EVOLUTION® Adaptive CS and PS Inserts; EVOLUTION® Revision CCK System; ADVANCE® Double High Insert; ADVANCE® A-CLASS® Tibial Insert; ADVANCE® Knee System; ADVANCE® Ultra-Congruent Tibial InseMicroport Orthopedics, 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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