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FDA 510(k)

NANOSS BONE VOID FILLER

K-Number: K050025 · 2005-02-03

ApplicantAngstrom Medica, Inc.
Decision Date2005-02-03
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NANOSS BONE VOID FILLER is the device name listed in this FDA 510(k) record. The listed applicant is Angstrom Medica, Inc.. It received FDA 510(k) clearance on 2005-02-03 under 510(k) number K050025. 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 NANOSS BONE VOID FILLER?

NANOSS BONE VOID FILLER is a medical device that received FDA 510(k) clearance on 2005-02-03. The listed applicant is Angstrom Medica, Inc.. The 510(k) number is K050025.

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

NANOSS BONE VOID FILLER received FDA 510(k) clearance on 2005-02-03, under 510(k) number K050025.

Who is the listed applicant for NANOSS BONE VOID FILLER?

The FDA 510(k) record lists Angstrom Medica, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

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

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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

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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