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PROCOTYL® PRIME Acetabular Cup System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170444
510(k) Type
Traditional
Applicant
MicroPort Orthopedics Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/2017
Days to Decision
132 days
Submission Type
Summary

PROCOTYL® PRIME Acetabular Cup System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170444
510(k) Type
Traditional
Applicant
MicroPort Orthopedics Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/2017
Days to Decision
132 days
Submission Type
Summary