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FDA 510(k)

MEDICAL INTERPOROUS

K-Number: K051342 · 2006-06-02

ApplicantBonyf AG
Decision Date2006-06-02
Product CodeEFT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MEDICAL INTERPOROUS is the device name listed in this FDA 510(k) record. The listed applicant is Bonyf AG. It received FDA 510(k) clearance on 2006-06-02 under 510(k) number K051342. The device is classified under product code EFT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICAL INTERPOROUS?

MEDICAL INTERPOROUS is a medical device that received FDA 510(k) clearance on 2006-06-02. The listed applicant is Bonyf AG. The 510(k) number is K051342.

When did MEDICAL INTERPOROUS receive FDA 510(k) clearance?

MEDICAL INTERPOROUS received FDA 510(k) clearance on 2006-06-02, under 510(k) number K051342.

Who is the listed applicant for MEDICAL INTERPOROUS?

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

What is the FDA product code for MEDICAL INTERPOROUS?

The FDA product code for MEDICAL INTERPOROUS is EFT.

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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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