MATRISTEM WOUND MATRIX
K-Number: K112409 · 2011-08-29
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Device Summary
Frequently Asked Questions
What is the MATRISTEM WOUND MATRIX?
MATRISTEM WOUND MATRIX is a medical device that received FDA 510(k) clearance on 2011-08-29. The listed applicant is Acell, Inc.. The 510(k) number is K112409.
When did MATRISTEM WOUND MATRIX receive FDA 510(k) clearance?
MATRISTEM WOUND MATRIX received FDA 510(k) clearance on 2011-08-29, under 510(k) number K112409.
Who is the listed applicant for MATRISTEM WOUND MATRIX?
The FDA 510(k) record lists Acell, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MATRISTEM WOUND MATRIX?
The FDA product code for MATRISTEM WOUND MATRIX is KGN.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Acell, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KGN)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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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