Reprocessed Covidien Trocar
K-Number: K172093 · 2017-10-05
ApplicantRenovo, Inc.
Decision Date2017-10-05
Product CodeNLM
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Reprocessed Covidien Trocar is a medical device manufactured by Renovo, Inc.. It received FDA 510(k) clearance on 2017-10-05 under approval number K172093. The device is classified under product code NLM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Reprocessed Covidien Trocar?
Reprocessed Covidien Trocar is a medical device that received FDA 510(k) clearance on 2017-10-05. It is manufactured by Renovo, Inc.. The 510(k) number is K172093.
When was Reprocessed Covidien Trocar approved by the FDA?
Reprocessed Covidien Trocar received FDA 510(k) clearance on 2017-10-05, under approval number K172093.
What company makes Reprocessed Covidien Trocar?
Reprocessed Covidien Trocar is manufactured by Renovo, Inc..
What is the FDA product code for Reprocessed Covidien Trocar?
The FDA product code for Reprocessed Covidien Trocar is NLM.
Other Devices by Renovo, Inc.
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K172097Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar SleevesRenovo, Inc.
K182828Medline ReNewal Reprocessed Carter-Thomason Needle Point Suture PasserSurgical Instrument Service and Savings, 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.