HAnano InterFuse(R) Modular Interbody
K-Number: K242509 · 2024-09-19
ApplicantNext Orthosurgical
Decision Date2024-09-19
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
HAnano InterFuse(R) Modular Interbody is a medical device manufactured by Next Orthosurgical. It received FDA 510(k) clearance on 2024-09-19 under approval number K242509. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the HAnano InterFuse(R) Modular Interbody?
HAnano InterFuse(R) Modular Interbody is a medical device that received FDA 510(k) clearance on 2024-09-19. It is manufactured by Next Orthosurgical. The 510(k) number is K242509.
When was HAnano InterFuse(R) Modular Interbody approved by the FDA?
HAnano InterFuse(R) Modular Interbody received FDA 510(k) clearance on 2024-09-19, under approval number K242509.
What company makes HAnano InterFuse(R) Modular Interbody?
HAnano InterFuse(R) Modular Interbody is manufactured by Next Orthosurgical.
What is the FDA product code for HAnano InterFuse(R) Modular Interbody?
The FDA product code for HAnano InterFuse(R) Modular Interbody is MAX.
Other Devices by Next Orthosurgical
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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.