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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 the device name listed in this FDA 510(k) record. The listed applicant is Curasan AG. It received FDA 510(k) clearance on 2016-12-02 under 510(k) 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. The listed applicant is Curasan AG. The 510(k) number is K160566.

When did Cerasorb Ortho Foam receive FDA 510(k) clearance?

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

Who is the listed applicant for Cerasorb Ortho Foam?

The FDA 510(k) record lists Curasan AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Cerasorb Ortho Foam?

The FDA product code for Cerasorb Ortho Foam is MQV.

Other records listing Curasan AG 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.

K181721Ceracell Ortho Foam

Related Devices (Code: MQV)

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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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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