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FDA 510(k)

MODIFICATION TO BONE GRAFT WASHER

K-Number: K041217 · 2004-05-28

ApplicantMedtronic Sofamor Danek, Inc.
Decision Date2004-05-28
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO BONE GRAFT WASHER is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Sofamor Danek, Inc.. It received FDA 510(k) clearance on 2004-05-28 under 510(k) number K041217. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO BONE GRAFT WASHER?

MODIFICATION TO BONE GRAFT WASHER is a medical device that received FDA 510(k) clearance on 2004-05-28. The listed applicant is Medtronic Sofamor Danek, Inc.. The 510(k) number is K041217.

When did MODIFICATION TO BONE GRAFT WASHER receive FDA 510(k) clearance?

MODIFICATION TO BONE GRAFT WASHER received FDA 510(k) clearance on 2004-05-28, under 510(k) number K041217.

Who is the listed applicant for MODIFICATION TO BONE GRAFT WASHER?

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

What is the FDA product code for MODIFICATION TO BONE GRAFT WASHER?

The FDA product code for MODIFICATION TO BONE GRAFT WASHER is KWQ.

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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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