Fitbone Trochanteric
K-Number: K233867 · 2024-06-18
ApplicantOrthofix Srl
Decision Date2024-06-18
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Fitbone Trochanteric is a medical device manufactured by Orthofix Srl. It received FDA 510(k) clearance on 2024-06-18 under approval number K233867. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Fitbone Trochanteric?
Fitbone Trochanteric is a medical device that received FDA 510(k) clearance on 2024-06-18. It is manufactured by Orthofix Srl. The 510(k) number is K233867.
When was Fitbone Trochanteric approved by the FDA?
Fitbone Trochanteric received FDA 510(k) clearance on 2024-06-18, under approval number K233867.
What company makes Fitbone Trochanteric?
Fitbone Trochanteric is manufactured by Orthofix Srl.
What is the FDA product code for Fitbone Trochanteric?
The FDA product code for Fitbone Trochanteric is HSB.
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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.