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FDA 510(k)

Cerasorb Ortho Foam

K-Number: K160566 · 2016-12-02

ApplicantCurasan AG
Decision Date2016-12-02
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Cerasorb Ortho Foam is a medical device manufactured by Curasan AG. It received FDA 510(k) clearance on 2016-12-02 under approval number K160566. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Cerasorb Ortho Foam?

Cerasorb Ortho Foam is a medical device that received FDA 510(k) clearance on 2016-12-02. It is manufactured by Curasan AG. The 510(k) number is K160566.

When was Cerasorb Ortho Foam approved by the FDA?

Cerasorb Ortho Foam received FDA 510(k) clearance on 2016-12-02, under approval number K160566.

What company makes Cerasorb Ortho Foam?

Cerasorb Ortho Foam is manufactured by Curasan AG.

What is the FDA product code for Cerasorb Ortho Foam?

The FDA product code for Cerasorb Ortho Foam is MQV.

Other Devices by Curasan AG

K181721Ceracell Ortho Foam

Related Devices (Code: MQV)

K160446MCP Bone PuttyBiostructures, LLC K161351NanoBone SBX PuttyArtoss GmbH K161447HydroSet XTOrthovita, Inc. K152077MaxiGenHans Biomed Corp. K151271BellaFuseHans Biomed Corp. K153608Vitoss BiModal Bone Graft Substitute Foam StripOrthovita, Inc.

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.

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