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FDA 510(k)

MEDTRONIC CLIP GUN KIT

K-Number: K050044 · 2005-02-07

ApplicantMedtronic Neurosurgery
Decision Date2005-02-07
Product CodeHBO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC CLIP GUN KIT is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Neurosurgery. It received FDA 510(k) clearance on 2005-02-07 under 510(k) number K050044. The device is classified under product code HBO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRONIC CLIP GUN KIT?

MEDTRONIC CLIP GUN KIT is a medical device that received FDA 510(k) clearance on 2005-02-07. The listed applicant is Medtronic Neurosurgery. The 510(k) number is K050044.

When did MEDTRONIC CLIP GUN KIT receive FDA 510(k) clearance?

MEDTRONIC CLIP GUN KIT received FDA 510(k) clearance on 2005-02-07, under 510(k) number K050044.

Who is the listed applicant for MEDTRONIC CLIP GUN KIT?

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

What is the FDA product code for MEDTRONIC CLIP GUN KIT?

The FDA product code for MEDTRONIC CLIP GUN KIT is HBO.

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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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