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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 a medical device manufactured by Microport Orthopedics, Inc.. It received FDA 510(k) clearance on 2019-07-15 under approval 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. It is manufactured by Microport Orthopedics, Inc.. The 510(k) number is K190123.

When was MicroPort CoCr Femoral Heads approved by the FDA?

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

What company makes MicroPort CoCr Femoral Heads?

MicroPort CoCr Femoral Heads is manufactured by Microport Orthopedics, Inc..

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

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

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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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