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PFC SIGMA Knee System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182301
510(k) Type
Traditional
Applicant
DePuy Orthopaedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2019
Days to Decision
441 days
Submission Type
Summary

PFC SIGMA Knee System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182301
510(k) Type
Traditional
Applicant
DePuy Orthopaedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2019
Days to Decision
441 days
Submission Type
Summary