Symphony

FDA 510(k) K200413 · Aroa Biosurgery , Ltd.

Substantially Equivalent

510(k) numberK200413

Submission

Device name
Symphony
Applicant
Aroa Biosurgery , Ltd.
Mangere, NZ
Received
February 19, 2020
Decision date
July 29, 2020
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KGN – Wound Dressing With Animal-Derived Material(S)
Device class
Unclassified
Implant
Yes

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More from Geistlich Pharma AG

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K260669Endoform Dermal TemplateKGN · Traditional 06/24/2026SE
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K231305Endoform Dental MembraneNPL · Traditional 01/23/2024SE
K223373Enivo™BTA · Traditional 04/07/2023SE
K200502Myriad ParticlesKGN · Traditional 03/31/2021SE
K183398Endoform RestellaFTM · Traditional 04/11/2019SE
K181935Endoform Reconstructive Template - Non AbsorbableFTL · Traditional 12/04/2018SE
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Questions and answers

When was Symphony cleared by the FDA?

Symphony (K200413) received a 510(k) decision of Substantially Equivalent on July 29, 2020, 161 days after the submission was received.

What is the product code of K200413?

The FDA product code is KGN – Wound Dressing With Animal-Derived Material(S), a Unclassified device.