Straumann Jason Membrane
K-Number: K173562 · 2018-07-09
ApplicantInstitut Straumann AG
Decision Date2018-07-09
Product CodeNPL
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Straumann Jason Membrane is a medical device manufactured by Institut Straumann AG. It received FDA 510(k) clearance on 2018-07-09 under approval number K173562. The device is classified under product code NPL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Straumann Jason Membrane?
Straumann Jason Membrane is a medical device that received FDA 510(k) clearance on 2018-07-09. It is manufactured by Institut Straumann AG. The 510(k) number is K173562.
When was Straumann Jason Membrane approved by the FDA?
Straumann Jason Membrane received FDA 510(k) clearance on 2018-07-09, under approval number K173562.
What company makes Straumann Jason Membrane?
Straumann Jason Membrane is manufactured by Institut Straumann AG.
What is the FDA product code for Straumann Jason Membrane?
The FDA product code for Straumann Jason Membrane is NPL.
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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.