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SURFIX KNEE OSTEOTOMY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041601
510(k) Type
Traditional
Applicant
SURFIX TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/2004
Days to Decision
74 days
Submission Type
Summary

SURFIX KNEE OSTEOTOMY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041601
510(k) Type
Traditional
Applicant
SURFIX TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/2004
Days to Decision
74 days
Submission Type
Summary