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FDA 510(k)

U-CLIP DEVICE

K-Number: K062821 · 2006-12-19

ApplicantMedtronic Neurosurgery
Decision Date2006-12-19
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

U-CLIP DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Neurosurgery. It received FDA 510(k) clearance on 2006-12-19 under 510(k) number K062821. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the U-CLIP DEVICE?

U-CLIP DEVICE is a medical device that received FDA 510(k) clearance on 2006-12-19. The listed applicant is Medtronic Neurosurgery. The 510(k) number is K062821.

When did U-CLIP DEVICE receive FDA 510(k) clearance?

U-CLIP DEVICE received FDA 510(k) clearance on 2006-12-19, under 510(k) number K062821.

Who is the listed applicant for U-CLIP DEVICE?

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 U-CLIP DEVICE?

The FDA product code for U-CLIP DEVICE is FZP.

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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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