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SpineJack Expansion Kit

Page Type
Cleared 510(K)
510(k) Number
K202393
510(k) Type
Traditional
Applicant
Stryker Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/2020
Days to Decision
60 days
Submission Type
Summary

SpineJack Expansion Kit

Page Type
Cleared 510(K)
510(k) Number
K202393
510(k) Type
Traditional
Applicant
Stryker Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/2020
Days to Decision
60 days
Submission Type
Summary