MERRIES K-PHATE BONE GRAFT SUBSTITUTE
K-Number: K063157 · 2008-03-10
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Device Summary
Frequently Asked Questions
What is the MERRIES K-PHATE BONE GRAFT SUBSTITUTE?
MERRIES K-PHATE BONE GRAFT SUBSTITUTE is a medical device that received FDA 510(k) clearance on 2008-03-10. The listed applicant is Merries International, Inc.. The 510(k) number is K063157.
When did MERRIES K-PHATE BONE GRAFT SUBSTITUTE receive FDA 510(k) clearance?
MERRIES K-PHATE BONE GRAFT SUBSTITUTE received FDA 510(k) clearance on 2008-03-10, under 510(k) number K063157.
Who is the listed applicant for MERRIES K-PHATE BONE GRAFT SUBSTITUTE?
The FDA 510(k) record lists Merries International, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MERRIES K-PHATE BONE GRAFT SUBSTITUTE?
The FDA product code for MERRIES K-PHATE BONE GRAFT SUBSTITUTE 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 Merries International, Inc. 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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