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FDA 510(k)

HYALOMATRIX PA

K-Number: K073251 · 2007-12-14

ApplicantFidia Advanced Biopolymers Srl
Decision Date2007-12-14
Product CodeQSZ
DecisionSubstantially Equivalent

Device Summary

HYALOMATRIX PA is the device name listed in this FDA 510(k) record. The listed applicant is Fidia Advanced Biopolymers Srl. It received FDA 510(k) clearance on 2007-12-14 under 510(k) number K073251. The device is classified under product code QSZ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYALOMATRIX PA?

HYALOMATRIX PA is a medical device that received FDA 510(k) clearance on 2007-12-14. The listed applicant is Fidia Advanced Biopolymers Srl. The 510(k) number is K073251.

When did HYALOMATRIX PA receive FDA 510(k) clearance?

HYALOMATRIX PA received FDA 510(k) clearance on 2007-12-14, under 510(k) number K073251.

Who is the listed applicant for HYALOMATRIX PA?

The FDA 510(k) record lists Fidia Advanced Biopolymers Srl as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HYALOMATRIX PA?

The FDA product code for HYALOMATRIX PA is QSZ.

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.

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Other records listing Fidia Advanced Biopolymers Srl 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.

K092257JALOSKINK001508LASERSKIN DRESSINGK003855HYALOMATRIX CO

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.

K261311HYALOMATRIXAnika Therapeutics, Inc.K254256LUOFUCON® Wound MatrixHuizhou Foryou Medical Devices Co., Ltd.K260020Redermo Wound MatrixBeijing Kreate Medical Co., Ltd.K251567NovoSorb BTMPolynovo Biomaterials Pty, Ltd.K242149NovoSorb® MTXPolynovo Biomaterials Pty, Ltd.K241660SiOxD® Wound MatrixSioxmed, LLC

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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