NanoBone SBX PUTTY, NanoBone QD
K-Number: K190110 · 2019-04-23
ApplicantArtoss GmbH
Decision Date2019-04-23
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
NanoBone SBX PUTTY, NanoBone QD is a medical device manufactured by Artoss GmbH. It received FDA 510(k) clearance on 2019-04-23 under approval number K190110. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NanoBone SBX PUTTY, NanoBone QD?
NanoBone SBX PUTTY, NanoBone QD is a medical device that received FDA 510(k) clearance on 2019-04-23. It is manufactured by Artoss GmbH. The 510(k) number is K190110.
When was NanoBone SBX PUTTY, NanoBone QD approved by the FDA?
NanoBone SBX PUTTY, NanoBone QD received FDA 510(k) clearance on 2019-04-23, under approval number K190110.
What company makes NanoBone SBX PUTTY, NanoBone QD?
NanoBone SBX PUTTY, NanoBone QD is manufactured by Artoss GmbH.
What is the FDA product code for NanoBone SBX PUTTY, NanoBone QD?
The FDA product code for NanoBone SBX PUTTY, NanoBone QD is MQV.
Other Devices by Artoss GmbH
Related Devices (Code: MQV)
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.