Nunchaku
K-Number: K161373 · 2016-11-03
Decision Date2016-11-03
Product CodeOKS
DecisionSubstantially Equivalent
Device Summary
Nunchaku is a medical device manufactured by Fci (France Chirurgie Instrumentation). It received FDA 510(k) clearance on 2016-11-03 under approval number K161373. The device is classified under product code OKS. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Nunchaku?
Nunchaku is a medical device that received FDA 510(k) clearance on 2016-11-03. It is manufactured by Fci (France Chirurgie Instrumentation). The 510(k) number is K161373.
When was Nunchaku approved by the FDA?
Nunchaku received FDA 510(k) clearance on 2016-11-03, under approval number K161373.
What company makes Nunchaku?
Nunchaku is manufactured by Fci (France Chirurgie Instrumentation).
What is the FDA product code for Nunchaku?
The FDA product code for Nunchaku is OKS.
Related Devices (Code: OKS)
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.