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FDA 510(k)

Geistlich Wound Matrix

K-Number: K171842 · 2017-11-03

ApplicantGeistlich Pharma AG
Decision Date2017-11-03
Product CodeKGN
DecisionSubstantially Equivalent

Device Summary

Geistlich Wound Matrix is a medical device manufactured by Geistlich Pharma AG. It received FDA 510(k) clearance on 2017-11-03 under approval number K171842. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Geistlich Wound Matrix?

Geistlich Wound Matrix is a medical device that received FDA 510(k) clearance on 2017-11-03. It is manufactured by Geistlich Pharma AG. The 510(k) number is K171842.

When was Geistlich Wound Matrix approved by the FDA?

Geistlich Wound Matrix received FDA 510(k) clearance on 2017-11-03, under approval number K171842.

What company makes Geistlich Wound Matrix?

Geistlich Wound Matrix is manufactured by Geistlich Pharma AG.

What is the FDA product code for Geistlich Wound Matrix?

The FDA product code for Geistlich Wound Matrix is KGN.

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Other Devices by Geistlich Pharma AG

K171050Geistlich Fibro-Gide K171643Geistlich Bio-Gide Shape, Geistlich Bio-Gide Compressed K182838Geistlich Derma-Gide 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) K203496Nexo-Gide Bilayer Collagen Membrane

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Related Devices (Code: KGN)

K160136Flowable Wound MatrixCook Biotech Incorporated K152600Collagen Dental Wound DressingsCollagen Matrix, Inc. K153754MicroMatrixAcell, Inc. K153690PriMatrix Dermal Repair ScaffoldTei Biosciences, Inc. K172010gel-e BandageGel-E, Inc. (Formerly Remedium Technologies, Inc.) K172399MicroMatrixAcell, Inc.

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.

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