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FDA 510(k)

SURGINETICS ADVANTAGEBLADE

K-Number: K062350 · 2007-02-26

ApplicantSurginetics
Decision Date2007-02-26
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGINETICS ADVANTAGEBLADE is the device name listed in this FDA 510(k) record. The listed applicant is Surginetics. It received FDA 510(k) clearance on 2007-02-26 under 510(k) number K062350. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGINETICS ADVANTAGEBLADE?

SURGINETICS ADVANTAGEBLADE is a medical device that received FDA 510(k) clearance on 2007-02-26. The listed applicant is Surginetics. The 510(k) number is K062350.

When did SURGINETICS ADVANTAGEBLADE receive FDA 510(k) clearance?

SURGINETICS ADVANTAGEBLADE received FDA 510(k) clearance on 2007-02-26, under 510(k) number K062350.

Who is the listed applicant for SURGINETICS ADVANTAGEBLADE?

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

What is the FDA product code for SURGINETICS ADVANTAGEBLADE?

The FDA product code for SURGINETICS ADVANTAGEBLADE is GEI.

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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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