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

Page Type
Cleared 510(K)
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)
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