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FDA 510(k)

MicroPort CoCr Femoral Heads

K-Number: K190123 · 2019-07-15

ApplicantMicroport Orthopedics, Inc.
Decision Date2019-07-15
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MicroPort CoCr Femoral Heads is the device name listed in this FDA 510(k) record. The listed applicant is Microport Orthopedics, Inc.. It received FDA 510(k) clearance on 2019-07-15 under 510(k) number K190123. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MicroPort CoCr Femoral Heads?

MicroPort CoCr Femoral Heads is a medical device that received FDA 510(k) clearance on 2019-07-15. The listed applicant is Microport Orthopedics, Inc.. The 510(k) number is K190123.

When did MicroPort CoCr Femoral Heads receive FDA 510(k) clearance?

MicroPort CoCr Femoral Heads received FDA 510(k) clearance on 2019-07-15, under 510(k) number K190123.

Who is the listed applicant for MicroPort CoCr Femoral Heads?

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

What is the FDA product code for MicroPort CoCr Femoral Heads?

The FDA product code for MicroPort CoCr Femoral Heads is LPH.

Other records listing Microport Orthopedics, Inc. as applicant

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Related Devices (Code: LPH)

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.

K254043TRIVANCE™ Hip StemGlobus Medical, Inc.K261624Omnifit® 20° Series I Insert;Omnifit® Crossfire® 10° Series II Insert; Constrained Acetabular Insert; Trident® Crossfire® 0° Polyethylene Insert; Trident ® Crossfire ® 10° Polyethylene Insert;System 12 Crossfire® 10° Insert; Trident® 0° Constrained Acetabular Insert; Trident® Constrained Acetabular Liner;Trident® All Poly Constrained Acetabular Insert; Crossfire® Eccentric Insert 10°; Artisan® Bone Plug;UHR® Universal Head Bipolar ComponentHowmedica Osteonics Corp., Dba Stryker OrthopaedicsK243192iNSitu Lateralized Acetabular Liners, iNSitu Femoral Stems with Plasma Sprayed CPTi CoatingNextstep Arthopedix, LLCK251270Taperloc® Complete Hip StemBiomet, Inc.K252623G7® Revision Acetabular SystemZimmer, Inc.K251043Mpact 3D Metal Implants Extension – DMLS TechnologyMedacta International S.A.

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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