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KMTI Hip Replacement System, Tesera Trabecular Technologies (T3) Acetabular Shell System, Porous Acetabular Cup System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201660
510(k) Type
Special
Applicant
Kyocera Medical Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/2020
Days to Decision
28 days
Submission Type
Summary

KMTI Hip Replacement System, Tesera Trabecular Technologies (T3) Acetabular Shell System, Porous Acetabular Cup System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201660
510(k) Type
Special
Applicant
Kyocera Medical Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/2020
Days to Decision
28 days
Submission Type
Summary