BONESAVE BONE VOID FILLER
K-Number: K033258 · 2004-03-09
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Device Summary
Frequently Asked Questions
What is the BONESAVE BONE VOID FILLER?
BONESAVE BONE VOID FILLER is a medical device that received FDA 510(k) clearance on 2004-03-09. The listed applicant is Howmedica Osteonics. The 510(k) number is K033258.
When did BONESAVE BONE VOID FILLER receive FDA 510(k) clearance?
BONESAVE BONE VOID FILLER received FDA 510(k) clearance on 2004-03-09, under 510(k) number K033258.
Who is the listed applicant for BONESAVE BONE VOID FILLER?
The FDA 510(k) record lists Howmedica Osteonics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BONESAVE BONE VOID FILLER?
The FDA product code for BONESAVE 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 Howmedica Osteonics 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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