Last synced on 16 May 2025 at 11:05 pm

Renova Spine Balloon Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231340
510(k) Type
Traditional
Applicant
Biopsybell s.r.l.
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
10/30/2023
Days to Decision
174 days
Submission Type
Summary

Renova Spine Balloon Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231340
510(k) Type
Traditional
Applicant
Biopsybell s.r.l.
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
10/30/2023
Days to Decision
174 days
Submission Type
Summary