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SERIES II X3 LARGE DIAMETER ACCETABULAR INSERTS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103124
510(k) Type
Special
Applicant
Stryker Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2010
Days to Decision
28 days
Submission Type
Summary

SERIES II X3 LARGE DIAMETER ACCETABULAR INSERTS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103124
510(k) Type
Special
Applicant
Stryker Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2010
Days to Decision
28 days
Submission Type
Summary