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AxoGen Nerve Cap

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163446
510(k) Type
Traditional
Applicant
AxoGen Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2017
Days to Decision
243 days
Submission Type
Summary

AxoGen Nerve Cap

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163446
510(k) Type
Traditional
Applicant
AxoGen Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2017
Days to Decision
243 days
Submission Type
Summary