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DELTACUT (APPARATUS AND CANNULA)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063233
510(k) Type
Traditional
Applicant
Pajunk GmbH Medizintechnologie
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
4/30/2007
Days to Decision
187 days
Submission Type
Summary

DELTACUT (APPARATUS AND CANNULA)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063233
510(k) Type
Traditional
Applicant
Pajunk GmbH Medizintechnologie
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
4/30/2007
Days to Decision
187 days
Submission Type
Summary