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Exactech® Alteon® HA Femoral Stem

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162732
510(k) Type
Traditional
Applicant
EXACTECH INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/2017
Days to Decision
209 days
Submission Type
Summary

Exactech® Alteon® HA Femoral Stem

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162732
510(k) Type
Traditional
Applicant
EXACTECH INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/2017
Days to Decision
209 days
Submission Type
Summary