NovoSorb Matrix— 510(k) K221686

Name: FDA 510(k) clearance K221686
Creator: U.S. Food and Drug Administration
Published: 2022-09-15

Substantially Equivalent

Polynovo Biomaterials Pty, Ltd.

FDA 510(k) clearance K221686 for NovoSorb Matrix, Substantially Equivalent on 2022-09-15. Applicant: Polynovo Biomaterials Pty, Ltd.. Device class: Unclassified.

Clearance details

Applicant: Polynovo Biomaterials Pty, Ltd.
Product code: Code QSZ
Device class: Unclassified
Advisory panel: Unknown
Date received: 2022-06-10
Decision date: 2022-09-15
Decision: Substantially Equivalent
Clearance type: Special
Location: Port Melbourne, AU

Download summary PDF View on FDA.gov ↗

Recent devices under product code QSZ

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K261311 — HYALOMATRIX2026-09-02
K254256 — LUOFUCON® Wound Matrix2026-08-18
K260020 — Redermo Wound Matrix2026-04-16
K251567 — NovoSorb BTM2025-06-20
K242149 — NovoSorb® MTX2025-03-05

More clearances from Polynovo Biomaterials Pty, Ltd.

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K172140 — NovoSorb BTM Wound Dressing (2cm x 2cm), NovoSorb BTM Wound Dressing (10cm x 10cm), NovoSorb BTM Wound Dressing (10cm x 20cm), NovoSorb BTM Wound Dressing (20cm x 40cm)2017-08-11
K142879 — BTM Wound Dressing2015-12-23
K132936 — NOVOPORE DRESSING2014-03-04

Data sourced from openFDA. This site is unofficial and independent of the FDA.