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AURORA® Surgiscope® System (ASX15/60); AURORA® Surgiscope® System (ASX15/80)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250752
510(k) Type
Special
Applicant
Integra LifeSciences Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2025
Days to Decision
28 days
Submission Type
Summary

AURORA® Surgiscope® System (ASX15/60); AURORA® Surgiscope® System (ASX15/80)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250752
510(k) Type
Special
Applicant
Integra LifeSciences Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2025
Days to Decision
28 days
Submission Type
Summary