Last synced on 23 September 2022 at 11:05 pm

Veloxion System, Veloxion Controller Kit, Veloxion Resecting Device Kit, Veloxion Fluid Control Set, Veloxion Saline Pole

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180752
510(k) Type
Traditional
Applicant
Corinth MedTech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2018
Days to Decision
125 days
Submission Type
Summary

Veloxion System, Veloxion Controller Kit, Veloxion Resecting Device Kit, Veloxion Fluid Control Set, Veloxion Saline Pole

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K180752
510(k) Type
Traditional
Applicant
Corinth MedTech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2018
Days to Decision
125 days
Submission Type
Summary