Last synced on 16 May 2025 at 11:05 pm

SpineJack Expansion Kit, Vertaplex Radiopaque Bone Cement, Vertaplex HV Radiopaque Bone Cement

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211238
510(k) Type
Traditional
Applicant
Stryker Instruments
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/2021
Days to Decision
60 days
Submission Type
Summary

SpineJack Expansion Kit, Vertaplex Radiopaque Bone Cement, Vertaplex HV Radiopaque Bone Cement

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211238
510(k) Type
Traditional
Applicant
Stryker Instruments
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/2021
Days to Decision
60 days
Submission Type
Summary