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EVOLUTION MP Revision Femur, EVOLUTION Femoral Augments

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142550
510(k) Type
Traditional
Applicant
MICROPORT ORTHOPEDICS INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/2014
Days to Decision
58 days
Submission Type
Summary

EVOLUTION MP Revision Femur, EVOLUTION Femoral Augments

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142550
510(k) Type
Traditional
Applicant
MICROPORT ORTHOPEDICS INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/2014
Days to Decision
58 days
Submission Type
Summary