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BIOFOAM® Additive Manufacturing (BIOFOAM® AM), ADVANCE® BIOFOAM® Tibial Base, EVOLUTION® BIOFOAM® Tibial Base, DYNASTY® BIOFOAM® Acetabular Shell

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170288
510(k) Type
Traditional
Applicant
MicroPort Orthopedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/2017
Days to Decision
136 days
Submission Type
Summary

BIOFOAM® Additive Manufacturing (BIOFOAM® AM), ADVANCE® BIOFOAM® Tibial Base, EVOLUTION® BIOFOAM® Tibial Base, DYNASTY® BIOFOAM® Acetabular Shell

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170288
510(k) Type
Traditional
Applicant
MicroPort Orthopedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/2017
Days to Decision
136 days
Submission Type
Summary