OSTEO-G BONE VOID FILLER SYSTEM
K-Number: K031319 · 2003-07-17
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Device Summary
Frequently Asked Questions
What is the OSTEO-G BONE VOID FILLER SYSTEM?
OSTEO-G BONE VOID FILLER SYSTEM is a medical device that received FDA 510(k) clearance on 2003-07-17. The listed applicant is Aspine USA, Inc.. The 510(k) number is K031319.
When did OSTEO-G BONE VOID FILLER SYSTEM receive FDA 510(k) clearance?
OSTEO-G BONE VOID FILLER SYSTEM received FDA 510(k) clearance on 2003-07-17, under 510(k) number K031319.
Who is the listed applicant for OSTEO-G BONE VOID FILLER SYSTEM?
The FDA 510(k) record lists Aspine USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OSTEO-G BONE VOID FILLER SYSTEM?
The FDA product code for OSTEO-G BONE VOID FILLER SYSTEM 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.
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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