Atlas FDA

NovoSorb Matrix

FDA 510(k) clearance K221686 · decided 2022-09-15

Clearance details

K-number
K221686
Device name
NovoSorb Matrix
Applicant
Polynovo Biomaterials Pty, Ltd.
Decision
Substantially Equivalent
Date received
2022-06-10
Decision date
2022-09-15
Days to decision
97 days
Clearance type
Special
Product code
QSZ
Device class
U
Medical specialty
Unknown
Advisory committee
Unknown
Location
Port Melbourne, AU
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Redermo Wound Matrix (K260020)Beijing Kreate Medical Co., Ltd.2026-04-16
NovoSorb BTM (K251567)Polynovo Biomaterials Pty, Ltd.2025-06-20
NovoSorb® MTX (K242149)Polynovo Biomaterials Pty, Ltd.2025-03-05
SiOxD® Wound Matrix (K241660)Sioxmed, LLC2024-07-05
SiOxD Wound Matrix (K232847)Sioxmed, LLC2023-12-18
Restrata® MiniMatrix (K223725)Acera Surgical, Inc.2023-05-18
SiOxD Wound Matrix (K222189)Sioxmed, LLC2022-11-18
Restrata® (K193583)Acera Surgical, Inc.2020-09-25
Phoenix Wound Matrix (K173544)Nanofiber Solutions, Inc.2018-03-02
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) (K172140)Polynovo Biomaterials Pty, Ltd.2017-08-11
SupraSDRM Biodegradable Matrix Wound Dressing (K170213)Polymedics Innovations, GmbH2017-06-28
Restrata Wound Matrix (K170300)Acera Surgical, Inc.2017-04-26

Recalls involving this device

No recalls on record reference this clearance.