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Prime BIOFOAM® Multi-Hole Shells

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201157
510(k) Type
Traditional
Applicant
MicroPort Orthopedics Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2021
Days to Decision
481 days
Submission Type
Summary

Prime BIOFOAM® Multi-Hole Shells

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201157
510(k) Type
Traditional
Applicant
MicroPort Orthopedics Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2021
Days to Decision
481 days
Submission Type
Summary