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Stryker iVAS Elite Inflatable Vertebral Augmentation System (Stryker iVAS Elite Balloon Catheter)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181752
510(k) Type
Traditional
Applicant
Stryker Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2018
Days to Decision
172 days
Submission Type
Summary

Stryker iVAS Elite Inflatable Vertebral Augmentation System (Stryker iVAS Elite Balloon Catheter)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181752
510(k) Type
Traditional
Applicant
Stryker Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2018
Days to Decision
172 days
Submission Type
Summary