Last synced on 30 May 2025 at 11:05 pm

Vertaplex HV High Viscosity Radiopaque Bone Cement; ES2 Augmentable Spinal System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192818
510(k) Type
Traditional
Applicant
Stryker Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2020
Days to Decision
182 days
Submission Type
Summary

Vertaplex HV High Viscosity Radiopaque Bone Cement; ES2 Augmentable Spinal System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192818
510(k) Type
Traditional
Applicant
Stryker Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2020
Days to Decision
182 days
Submission Type
Summary