Geistlich Wound Matrix PLUS
K-Number: K213607 · 2022-04-28
ApplicantGeistlich Pharma AG
Decision Date2022-04-28
Product CodeKGN
DecisionSubstantially Equivalent
Device Summary
Geistlich Wound Matrix PLUS is a medical device manufactured by Geistlich Pharma AG. It received FDA 510(k) clearance on 2022-04-28 under approval number K213607. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Geistlich Wound Matrix PLUS?
Geistlich Wound Matrix PLUS is a medical device that received FDA 510(k) clearance on 2022-04-28. It is manufactured by Geistlich Pharma AG. The 510(k) number is K213607.
When was Geistlich Wound Matrix PLUS approved by the FDA?
Geistlich Wound Matrix PLUS received FDA 510(k) clearance on 2022-04-28, under approval number K213607.
What company makes Geistlich Wound Matrix PLUS?
Geistlich Wound Matrix PLUS is manufactured by Geistlich Pharma AG.
What is the FDA product code for Geistlich Wound Matrix PLUS?
The FDA product code for Geistlich Wound Matrix PLUS is KGN.
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Other Devices by Geistlich Pharma AG
K171050Geistlich Fibro-Gide
K171842Geistlich Wound Matrix
K171643Geistlich Bio-Gide Shape, Geistlich Bio-Gide Compressed
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K192042Geistlich Bio-Gide, Geistlich Bio-Gide Shape, Geistlich Bio-Gide Compressed, Geistlich Bio-Gide Perio, Geistlich Combi-Kit Collagen, Geistlich Perio-System Combi-Pack, Geistlich Mucograft and Geistlich Mucograft Seal
K190754Orthoss(R)
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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.