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Acculoc Total Knee System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182370
510(k) Type
Special
Applicant
Rootloc Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
9/27/2018
Days to Decision
27 days
Submission Type
Summary

Acculoc Total Knee System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182370
510(k) Type
Special
Applicant
Rootloc Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
9/27/2018
Days to Decision
27 days
Submission Type
Summary