MASTERGRAFT PUTTY BONE VOID FILLER
K-Number: K051386 · 2005-12-16
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Device Summary
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.
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
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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