NovoSorb Matrix
K-Number: K221686 · 2022-09-15
Device Summary
Frequently Asked Questions
What is the NovoSorb Matrix?
NovoSorb Matrix is a medical device that received FDA 510(k) clearance on 2022-09-15. The listed applicant is Polynovo Biomaterials Pty, Ltd.. The 510(k) number is K221686.
When did NovoSorb Matrix receive FDA 510(k) clearance?
NovoSorb Matrix received FDA 510(k) clearance on 2022-09-15, under 510(k) number K221686.
Who is the listed applicant for NovoSorb Matrix?
The FDA 510(k) record lists Polynovo Biomaterials Pty, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NovoSorb Matrix?
The FDA product code for NovoSorb Matrix is QSZ.
Other records listing Polynovo Biomaterials Pty, Ltd. 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: QSZ)
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.