FDA 510(k) Applications Submitted by AxoGen Corporation

FDA 510(k) Number Submission Date Device Name Applicant
K223640 12/05/2022 Axoguard HA+ Nerve Protector (AGHA12); Axoguard HA+ Nerve Protector (AGHA22); Axoguard HA+ Nerve Protector (AGHA24); Axoguard HA+ Nerve Protector (AGHA36); Axoguard HA+ Nerve Protector (AGHA48) AxoGen Corporation
K163446 12/08/2016 AxoGen Nerve Cap AxoGen Corporation


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