FDA 510(k)

COMPRESS DISTAL FEMORAL REPLACEMENT

K-Number: K031804 · 2003-12-18

Decision Date2003-12-18

Product CodeKRO

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

COMPRESS DISTAL FEMORAL REPLACEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2003-12-18 under 510(k) number K031804. 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 COMPRESS DISTAL FEMORAL REPLACEMENT?

COMPRESS DISTAL FEMORAL REPLACEMENT is a medical device that received FDA 510(k) clearance on 2003-12-18. The listed applicant is Biomet, Inc.. The 510(k) number is K031804.

When did COMPRESS DISTAL FEMORAL REPLACEMENT receive FDA 510(k) clearance?

COMPRESS DISTAL FEMORAL REPLACEMENT received FDA 510(k) clearance on 2003-12-18, under 510(k) number K031804.

Who is the listed applicant for COMPRESS DISTAL FEMORAL REPLACEMENT?

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

What is the FDA product code for COMPRESS DISTAL FEMORAL REPLACEMENT?

The FDA product code for COMPRESS DISTAL FEMORAL REPLACEMENT is KRO.

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Related Devices (Code: KRO)

K261898Triathlon® Knee System; Triathlon® Hinge Knee System; Scorpio® Total Knee SystemHowmedica Osteonics Corp. dba Stryker Orthopaedics K252898Triathlon® Tritanium® Asymmetric Patella; Triathlon® Tritanium® Symmetric Patella; Triathlon® Symmetric Patella; Triathlon® Asymmetric Patella; Scorpio® Universal Dome Patella; Triathlon® Hinge BumperHowmedica Osteonics Corp., Dba Stryker Orthopaedics K252303Stem Extension Line (USTAR II System)United Orthopedic Corporation K251665Triathlon® Hinge Knee SystemHowmedica Osteonics Corp., Dba Stryker Orthopaedics K242871ATTUNE™ Revision Hinge KneeDepuy Ireland UC K240043EVOLUTION® 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.