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Aesculap Video Assisted Thoracic Surgery (VATS) INstruments

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170683
510(k) Type
Traditional
Applicant
Aesculap, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/2018
Days to Decision
350 days
Submission Type
Summary