FDA 510(k)

NAME BONE VOID FILLER

K-Number: K041421 · 2004-08-26

Decision Date2004-08-26

Product CodeMQV

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

NAME BONE VOID FILLER is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Biotech. It received FDA 510(k) clearance on 2004-08-26 under 510(k) number K041421. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAME BONE VOID FILLER?

NAME BONE VOID FILLER is a medical device that received FDA 510(k) clearance on 2004-08-26. The listed applicant is Stryker Biotech. The 510(k) number is K041421.

When did NAME BONE VOID FILLER receive FDA 510(k) clearance?

NAME BONE VOID FILLER received FDA 510(k) clearance on 2004-08-26, under 510(k) number K041421.

Who is the listed applicant for NAME BONE VOID FILLER?

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

What is the FDA product code for NAME BONE VOID FILLER?

The FDA product code for NAME BONE VOID FILLER is MQV.

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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.