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UF(II) Implant System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170608
510(k) Type
Traditional
Applicant
Dio Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
3/30/2018
Days to Decision
394 days
Submission Type
Summary

UF(II) Implant System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170608
510(k) Type
Traditional
Applicant
Dio Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
3/30/2018
Days to Decision
394 days
Submission Type
Summary