A-GRIX TE RESORABLE BONE VOID FILLER
K-Number: K121453 · 2013-02-05
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Device Summary
Frequently Asked Questions
What is the A-GRIX TE RESORABLE BONE VOID FILLER?
A-GRIX TE RESORABLE BONE VOID FILLER is a medical device that received FDA 510(k) clearance on 2013-02-05. The listed applicant is Ag Digital Technology Corp.. The 510(k) number is K121453.
When did A-GRIX TE RESORABLE BONE VOID FILLER receive FDA 510(k) clearance?
A-GRIX TE RESORABLE BONE VOID FILLER received FDA 510(k) clearance on 2013-02-05, under 510(k) number K121453.
Who is the listed applicant for A-GRIX TE RESORABLE BONE VOID FILLER?
The FDA 510(k) record lists Ag Digital Technology Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for A-GRIX TE RESORABLE BONE VOID FILLER?
The FDA product code for A-GRIX TE RESORABLE 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 Ag Digital Technology Corp. 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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