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PROCOTYL® PRIME E-CLASS™ XLPE Liner

Page Type
Cleared 510(K)
510(k) Number
K171181
510(k) Type
Traditional
Applicant
MicroPort Orthopedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2017
Days to Decision
126 days
Submission Type
Summary

PROCOTYL® PRIME E-CLASS™ XLPE Liner

Page Type
Cleared 510(K)
510(k) Number
K171181
510(k) Type
Traditional
Applicant
MicroPort Orthopedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2017
Days to Decision
126 days
Submission Type
Summary