Rodo Abutment System
K-Number: K193274 · 2020-02-27
ApplicantRodo Medical, Inc.
Decision Date2020-02-27
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Rodo Abutment System is a medical device manufactured by Rodo Medical, Inc.. It received FDA 510(k) clearance on 2020-02-27 under approval number K193274. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Rodo Abutment System?
Rodo Abutment System is a medical device that received FDA 510(k) clearance on 2020-02-27. It is manufactured by Rodo Medical, Inc.. The 510(k) number is K193274.
When was Rodo Abutment System approved by the FDA?
Rodo Abutment System received FDA 510(k) clearance on 2020-02-27, under approval number K193274.
What company makes Rodo Abutment System?
Rodo Abutment System is manufactured by Rodo Medical, Inc..
What is the FDA product code for Rodo Abutment System?
The FDA product code for Rodo Abutment System is NHA.
Related Clinical Trials
Other Devices by Rodo Medical, Inc.
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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.