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FDA 510(k)

NOVABONE PUTTY - RESORBABLE BONE VOID FILLER

K-Number: K051617 · 2006-03-06

ApplicantNovabone Products, LLC
Decision Date2006-03-06
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NOVABONE PUTTY - RESORBABLE BONE VOID FILLER is the device name listed in this FDA 510(k) record. The listed applicant is Novabone Products, LLC. It received FDA 510(k) clearance on 2006-03-06 under 510(k) number K051617. 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 NOVABONE PUTTY - RESORBABLE BONE VOID FILLER?

NOVABONE PUTTY - RESORBABLE BONE VOID FILLER is a medical device that received FDA 510(k) clearance on 2006-03-06. The listed applicant is Novabone Products, LLC. The 510(k) number is K051617.

When did NOVABONE PUTTY - RESORBABLE BONE VOID FILLER receive FDA 510(k) clearance?

NOVABONE PUTTY - RESORBABLE BONE VOID FILLER received FDA 510(k) clearance on 2006-03-06, under 510(k) number K051617.

Who is the listed applicant for NOVABONE PUTTY - RESORBABLE BONE VOID FILLER?

The FDA 510(k) record lists Novabone Products, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NOVABONE PUTTY - RESORBABLE BONE VOID FILLER?

The FDA product code for NOVABONE PUTTY - RESORBABLE BONE VOID FILLER is MQV.

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Other records listing Novabone Products, LLC as applicant

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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.

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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.

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