Trivicta Hip Stem
K-Number: K233758 · 2024-03-08
ApplicantOrtho Development Corp.
Decision Date2024-03-08
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Trivicta Hip Stem is a medical device manufactured by Ortho Development Corp.. It received FDA 510(k) clearance on 2024-03-08 under approval number K233758. 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 Trivicta Hip Stem?
Trivicta Hip Stem is a medical device that received FDA 510(k) clearance on 2024-03-08. It is manufactured by Ortho Development Corp.. The 510(k) number is K233758.
When was Trivicta Hip Stem approved by the FDA?
Trivicta Hip Stem received FDA 510(k) clearance on 2024-03-08, under approval number K233758.
What company makes Trivicta Hip Stem?
Trivicta Hip Stem is manufactured by Ortho Development Corp..
What is the FDA product code for Trivicta Hip Stem?
The FDA product code for Trivicta Hip Stem is MEH.
Other Devices by Ortho Development Corp.
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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.