NanoHive Medical Lumbar Interbody System
K-Number: K231241 · 2023-07-12
ApplicantNanoHive Medical, LLC
Decision Date2023-07-12
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
NanoHive Medical Lumbar Interbody System is a medical device manufactured by NanoHive Medical, LLC. It received FDA 510(k) clearance on 2023-07-12 under approval number K231241. 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 NanoHive Medical Lumbar Interbody System?
NanoHive Medical Lumbar Interbody System is a medical device that received FDA 510(k) clearance on 2023-07-12. It is manufactured by NanoHive Medical, LLC. The 510(k) number is K231241.
When was NanoHive Medical Lumbar Interbody System approved by the FDA?
NanoHive Medical Lumbar Interbody System received FDA 510(k) clearance on 2023-07-12, under approval number K231241.
What company makes NanoHive Medical Lumbar Interbody System?
NanoHive Medical Lumbar Interbody System is manufactured by NanoHive Medical, LLC.
What is the FDA product code for NanoHive Medical Lumbar Interbody System?
The FDA product code for NanoHive Medical Lumbar Interbody System is MAX.
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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.