DePuy Actis DuoFix Hip Prosthesis
K-Number: K160907 · 2016-07-19
ApplicantDepuy(Ireland)
Decision Date2016-07-19
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
DePuy Actis DuoFix Hip Prosthesis is a medical device manufactured by Depuy(Ireland). It received FDA 510(k) clearance on 2016-07-19 under approval number K160907. 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 DePuy Actis DuoFix Hip Prosthesis?
DePuy Actis DuoFix Hip Prosthesis is a medical device that received FDA 510(k) clearance on 2016-07-19. It is manufactured by Depuy(Ireland). The 510(k) number is K160907.
When was DePuy Actis DuoFix Hip Prosthesis approved by the FDA?
DePuy Actis DuoFix Hip Prosthesis received FDA 510(k) clearance on 2016-07-19, under approval number K160907.
What company makes DePuy Actis DuoFix Hip Prosthesis?
DePuy Actis DuoFix Hip Prosthesis is manufactured by Depuy(Ireland).
What is the FDA product code for DePuy Actis DuoFix Hip Prosthesis?
The FDA product code for DePuy Actis DuoFix Hip Prosthesis 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.