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PathLoc-SI Joint Fusion System

Page Type
Cleared 510(K)
510(k) Number
K181600
510(k) Type
Special
Applicant
L&K BIOMED Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/16/2018
Days to Decision
28 days
Submission Type
Summary

PathLoc-SI Joint Fusion System

Page Type
Cleared 510(K)
510(k) Number
K181600
510(k) Type
Special
Applicant
L&K BIOMED Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/16/2018
Days to Decision
28 days
Submission Type
Summary