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FDA 510(k)

COLORADO MICRODISSECTION NEEDLE

K-Number: K033232 · 2004-02-25

ApplicantStryker Corp.
Decision Date2004-02-25
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

COLORADO MICRODISSECTION NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 2004-02-25 under 510(k) number K033232. 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 COLORADO MICRODISSECTION NEEDLE?

COLORADO MICRODISSECTION NEEDLE is a medical device that received FDA 510(k) clearance on 2004-02-25. The listed applicant is Stryker Corp.. The 510(k) number is K033232.

When did COLORADO MICRODISSECTION NEEDLE receive FDA 510(k) clearance?

COLORADO MICRODISSECTION NEEDLE received FDA 510(k) clearance on 2004-02-25, under 510(k) number K033232.

Who is the listed applicant for COLORADO MICRODISSECTION NEEDLE?

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

What is the FDA product code for COLORADO MICRODISSECTION NEEDLE?

The FDA product code for COLORADO MICRODISSECTION NEEDLE is GEI.

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Related Devices (Code: GEI)

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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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