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FDA 510(k)

MASTERGRAFT PUTTY BONE VOID FILLER

K-Number: K051386 · 2005-12-16

Decision Date2005-12-16
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MASTERGRAFT PUTTY BONE VOID FILLER is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 2005-12-16 under 510(k) number K051386. 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 MASTERGRAFT PUTTY BONE VOID FILLER?

MASTERGRAFT PUTTY BONE VOID FILLER is a medical device that received FDA 510(k) clearance on 2005-12-16. The listed applicant is Medtronic Vascular. The 510(k) number is K051386.

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

MASTERGRAFT PUTTY BONE VOID FILLER received FDA 510(k) clearance on 2005-12-16, under 510(k) number K051386.

Who is the listed applicant for MASTERGRAFT PUTTY BONE VOID FILLER?

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

What is the FDA product code for MASTERGRAFT PUTTY BONE VOID FILLER?

The FDA product code for MASTERGRAFT PUTTY BONE VOID FILLER is MQV.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Medtronic Vascular as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 474 devices →

Related Devices (Code: MQV)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

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