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FDA 510(k)

MEMOMETAL VARISATION, MODELS AV26-08, AV26-10, AV90-08 AND AV90-10

K-Number: K070033 · 2007-03-19

ApplicantMemometal Technologies
Decision Date2007-03-19
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MEMOMETAL VARISATION, MODELS AV26-08, AV26-10, AV90-08 AND AV90-10 is the device name listed in this FDA 510(k) record. The listed applicant is Memometal Technologies. It received FDA 510(k) clearance on 2007-03-19 under 510(k) number K070033. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEMOMETAL VARISATION, MODELS AV26-08, AV26-10, AV90-08 AND AV90-10?

MEMOMETAL VARISATION, MODELS AV26-08, AV26-10, AV90-08 AND AV90-10 is a medical device that received FDA 510(k) clearance on 2007-03-19. The listed applicant is Memometal Technologies. The 510(k) number is K070033.

When did MEMOMETAL VARISATION, MODELS AV26-08, AV26-10, AV90-08 AND AV90-10 receive FDA 510(k) clearance?

MEMOMETAL VARISATION, MODELS AV26-08, AV26-10, AV90-08 AND AV90-10 received FDA 510(k) clearance on 2007-03-19, under 510(k) number K070033.

Who is the listed applicant for MEMOMETAL VARISATION, MODELS AV26-08, AV26-10, AV90-08 AND AV90-10?

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

What is the FDA product code for MEMOMETAL VARISATION, MODELS AV26-08, AV26-10, AV90-08 AND AV90-10?

The FDA product code for MEMOMETAL VARISATION, MODELS AV26-08, AV26-10, AV90-08 AND AV90-10 is JDR.

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Other records listing Memometal Technologies as applicant

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Related Devices (Code: JDR)

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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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