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DISCYPHOR CATHETER SYSTEM, MODEL D01A; DISCYPHOR INTRODUCER NEEDLE, MODEL D01B

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063071
510(k) Type
Special
Applicant
Kyphon, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2007
Days to Decision
189 days
Submission Type
Summary

DISCYPHOR CATHETER SYSTEM, MODEL D01A; DISCYPHOR INTRODUCER NEEDLE, MODEL D01B

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063071
510(k) Type
Special
Applicant
Kyphon, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2007
Days to Decision
189 days
Submission Type
Summary