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SpineKure Kyphoplasty System

Page Type
Cleared 510(K)
510(k) Number
K172871
510(k) Type
Traditional
Applicant
Hanchang Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
5/29/2018
Days to Decision
250 days
Submission Type
Summary

SpineKure Kyphoplasty System

Page Type
Cleared 510(K)
510(k) Number
K172871
510(k) Type
Traditional
Applicant
Hanchang Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
5/29/2018
Days to Decision
250 days
Submission Type
Summary