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FDA 510(k)

MicroMatrix

K-Number: K172399 · 2017-10-06

ApplicantAcell, Inc.
Decision Date2017-10-06
Product CodeKGN
DecisionSubstantially Equivalent

Device Summary

MicroMatrix is a medical device manufactured by Acell, Inc.. It received FDA 510(k) clearance on 2017-10-06 under approval number K172399. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MicroMatrix?

MicroMatrix is a medical device that received FDA 510(k) clearance on 2017-10-06. It is manufactured by Acell, Inc.. The 510(k) number is K172399.

When was MicroMatrix approved by the FDA?

MicroMatrix received FDA 510(k) clearance on 2017-10-06, under approval number K172399.

What company makes MicroMatrix?

MicroMatrix is manufactured by Acell, Inc..

What is the FDA product code for MicroMatrix?

The FDA product code for MicroMatrix is KGN.

Other Devices by Acell, Inc.

K162554Gentrix Surgical Matrix K153754MicroMatrix K170763Gentrix Surgical Matrix Thick; Gentrix Surgical Matrix Extend K180776Cytal Wound Particulate K191734MatriStem UBM Pericardial Patch K192725Cytal Wound Matrix 3-Layer

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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.) K171842Geistlich Wound MatrixGeistlich Pharma AG

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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