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FDA 510(k)

VESAFITCUP DOUBLE MOBILITY- HIGHCROSS HXUHMWPE LINERS

K-Number: K092265 · 2010-03-12

ApplicantMedacta International S.A.
Decision Date2010-03-12
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VESAFITCUP DOUBLE MOBILITY- HIGHCROSS HXUHMWPE LINERS is the device name listed in this FDA 510(k) record. The listed applicant is Medacta International S.A.. It received FDA 510(k) clearance on 2010-03-12 under 510(k) number K092265. The device is classified under product code MEH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VESAFITCUP DOUBLE MOBILITY- HIGHCROSS HXUHMWPE LINERS?

VESAFITCUP DOUBLE MOBILITY- HIGHCROSS HXUHMWPE LINERS is a medical device that received FDA 510(k) clearance on 2010-03-12. The listed applicant is Medacta International S.A.. The 510(k) number is K092265.

When did VESAFITCUP DOUBLE MOBILITY- HIGHCROSS HXUHMWPE LINERS receive FDA 510(k) clearance?

VESAFITCUP DOUBLE MOBILITY- HIGHCROSS HXUHMWPE LINERS received FDA 510(k) clearance on 2010-03-12, under 510(k) number K092265.

Who is the listed applicant for VESAFITCUP DOUBLE MOBILITY- HIGHCROSS HXUHMWPE LINERS?

The FDA 510(k) record lists Medacta International S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VESAFITCUP DOUBLE MOBILITY- HIGHCROSS HXUHMWPE LINERS?

The FDA product code for VESAFITCUP DOUBLE MOBILITY- HIGHCROSS HXUHMWPE LINERS is MEH.

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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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