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PROLIXUS TOTAL KNEE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170534
510(k) Type
Traditional
Applicant
OTIS Biotech Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
11/9/2017
Days to Decision
259 days
Submission Type
Summary

PROLIXUS TOTAL KNEE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170534
510(k) Type
Traditional
Applicant
OTIS Biotech Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
11/9/2017
Days to Decision
259 days
Submission Type
Summary