Last synced on 25 January 2026 at 3:41 am

13G InterV Kyphoplasty Catheter (Micro) and 11G InterV Kyphoplasty Catheter (Mini-Flex)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162453
510(k) Type
Special
Applicant
Pan Medical , Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
11/1/2016
Days to Decision
61 days
Submission Type
Summary

13G InterV Kyphoplasty Catheter (Micro) and 11G InterV Kyphoplasty Catheter (Mini-Flex)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162453
510(k) Type
Special
Applicant
Pan Medical , Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
11/1/2016
Days to Decision
61 days
Submission Type
Summary