BONOS R 1X20, BONOS R 2X20, BONOS R 1X40, BONOS R 2X40, BONOS R 1X60
K-Number: K123225 · 2013-03-15
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Device Summary
Frequently Asked Questions
What is the BONOS R 1X20, BONOS R 2X20, BONOS R 1X40, BONOS R 2X40, BONOS R 1X60?
BONOS R 1X20, BONOS R 2X20, BONOS R 1X40, BONOS R 2X40, BONOS R 1X60 is a medical device that received FDA 510(k) clearance on 2013-03-15. The listed applicant is Aap Biomaterials GmbH & Co. KG. The 510(k) number is K123225.
When did BONOS R 1X20, BONOS R 2X20, BONOS R 1X40, BONOS R 2X40, BONOS R 1X60 receive FDA 510(k) clearance?
BONOS R 1X20, BONOS R 2X20, BONOS R 1X40, BONOS R 2X40, BONOS R 1X60 received FDA 510(k) clearance on 2013-03-15, under 510(k) number K123225.
Who is the listed applicant for BONOS R 1X20, BONOS R 2X20, BONOS R 1X40, BONOS R 2X40, BONOS R 1X60?
The FDA 510(k) record lists Aap Biomaterials GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BONOS R 1X20, BONOS R 2X20, BONOS R 1X40, BONOS R 2X40, BONOS R 1X60?
The FDA product code for BONOS R 1X20, BONOS R 2X20, BONOS R 1X40, BONOS R 2X40, BONOS R 1X60 is LOD.
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Other records listing Aap Biomaterials GmbH & Co. KG 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: LOD)
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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