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ACUMATCH P-SERIES POROUS PRESS-FIT FEMORAL COMPONENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030236
510(k) Type
Special
Applicant
EXACTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/2003
Days to Decision
28 days
Submission Type
Summary

ACUMATCH P-SERIES POROUS PRESS-FIT FEMORAL COMPONENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030236
510(k) Type
Special
Applicant
EXACTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/2003
Days to Decision
28 days
Submission Type
Summary