OSTEOFIX BONE VOID FILLER
K-Number: K070220 · 2007-04-12
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Device Summary
Frequently Asked Questions
What is the OSTEOFIX BONE VOID FILLER?
OSTEOFIX BONE VOID FILLER is a medical device that received FDA 510(k) clearance on 2007-04-12. The listed applicant is Calcitec, Inc.. The 510(k) number is K070220.
When did OSTEOFIX BONE VOID FILLER receive FDA 510(k) clearance?
OSTEOFIX BONE VOID FILLER received FDA 510(k) clearance on 2007-04-12, under 510(k) number K070220.
Who is the listed applicant for OSTEOFIX BONE VOID FILLER?
The FDA 510(k) record lists Calcitec, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OSTEOFIX BONE VOID FILLER?
The FDA product code for OSTEOFIX 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.
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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