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FDA 510(k)

ELLIPTIC MATRIX

K-Number: K040539 · 2004-03-18

ApplicantInstitut Straumann AG
Decision Date2004-03-18
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ELLIPTIC MATRIX is the device name listed in this FDA 510(k) record. The listed applicant is Institut Straumann AG. It received FDA 510(k) clearance on 2004-03-18 under 510(k) number K040539. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELLIPTIC MATRIX?

ELLIPTIC MATRIX is a medical device that received FDA 510(k) clearance on 2004-03-18. The listed applicant is Institut Straumann AG. The 510(k) number is K040539.

When did ELLIPTIC MATRIX receive FDA 510(k) clearance?

ELLIPTIC MATRIX received FDA 510(k) clearance on 2004-03-18, under 510(k) number K040539.

Who is the listed applicant for ELLIPTIC MATRIX?

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

What is the FDA product code for ELLIPTIC MATRIX?

The FDA product code for ELLIPTIC MATRIX is NHA.

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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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