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CRANIOFIX AND CRANIOFIX2 TITANIUM CLAMP SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040864
510(k) Type
Traditional
Applicant
AESCULAP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2004
Days to Decision
76 days
Submission Type
Summary

CRANIOFIX AND CRANIOFIX2 TITANIUM CLAMP SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040864
510(k) Type
Traditional
Applicant
AESCULAP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2004
Days to Decision
76 days
Submission Type
Summary