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KeYi Spinal Fixation System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190567
510(k) Type
Traditional
Applicant
Beijing Keyi Medical Device Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/8/2019
Days to Decision
63 days
Submission Type
Summary

KeYi Spinal Fixation System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190567
510(k) Type
Traditional
Applicant
Beijing Keyi Medical Device Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/8/2019
Days to Decision
63 days
Submission Type
Summary