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Vortex Surgical Laser Probes, Vortex Surgical Illuminated Laser Probes, Vortex Surgical Endoilluminators, Vortex Surgical Chandeliers

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220263
510(k) Type
Traditional
Applicant
Vortex Surgical Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/2022
Days to Decision
276 days
Submission Type
Summary

Vortex Surgical Laser Probes, Vortex Surgical Illuminated Laser Probes, Vortex Surgical Endoilluminators, Vortex Surgical Chandeliers

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220263
510(k) Type
Traditional
Applicant
Vortex Surgical Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/2022
Days to Decision
276 days
Submission Type
Summary