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FDA 510(k)

NOVABONE POROUS - SYNTHETIC BONE GRAFT SCAFFOLD

K-Number: K090731 · 2009-04-15

ApplicantNovabone Products, LLC
Decision Date2009-04-15
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NOVABONE POROUS - SYNTHETIC BONE GRAFT SCAFFOLD 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 2009-04-15 under 510(k) number K090731. 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 POROUS - SYNTHETIC BONE GRAFT SCAFFOLD?

NOVABONE POROUS - SYNTHETIC BONE GRAFT SCAFFOLD is a medical device that received FDA 510(k) clearance on 2009-04-15. The listed applicant is Novabone Products, LLC. The 510(k) number is K090731.

When did NOVABONE POROUS - SYNTHETIC BONE GRAFT SCAFFOLD receive FDA 510(k) clearance?

NOVABONE POROUS - SYNTHETIC BONE GRAFT SCAFFOLD received FDA 510(k) clearance on 2009-04-15, under 510(k) number K090731.

Who is the listed applicant for NOVABONE POROUS - SYNTHETIC BONE GRAFT SCAFFOLD?

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 POROUS - SYNTHETIC BONE GRAFT SCAFFOLD?

The FDA product code for NOVABONE POROUS - SYNTHETIC BONE GRAFT SCAFFOLD 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.

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