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FDA 510(k)

Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars

K-Number: K153258 · 2016-04-05

Decision Date2016-04-05
Product CodeNLM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars is a medical device manufactured by Surgical Instrument Service and Savings (Dba Medline Renewal. It received FDA 510(k) clearance on 2016-04-05 under approval number K153258. 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 Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars?

Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars is a medical device that received FDA 510(k) clearance on 2016-04-05. It is manufactured by Surgical Instrument Service and Savings (Dba Medline Renewal. The 510(k) number is K153258.

When was Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars approved by the FDA?

Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars received FDA 510(k) clearance on 2016-04-05, under approval number K153258.

What company makes Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars?

Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars is manufactured by Surgical Instrument Service and Savings (Dba Medline Renewal.

What is the FDA product code for Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars?

The FDA product code for Medline ReNewal Reprocessed Versaport V2 Bladeless Optical Trocars is NLM.

Related Devices (Code: NLM)

Official Source

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