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PIPELINE CR PRIMARY KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K113122
510(k) Type
Traditional
Applicant
PIPELINE ORTHOPEDICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2012
Days to Decision
151 days
Submission Type
Summary

PIPELINE CR PRIMARY KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K113122
510(k) Type
Traditional
Applicant
PIPELINE ORTHOPEDICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2012
Days to Decision
151 days
Submission Type
Summary