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DISCYPHOR DIRECT CATHETER SYSTEM, DISCYPHOR DIRECT NEEDLES, LONG, DISCYPHOR DIRECT NEEDLES, REGULAR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073516
510(k) Type
Traditional
Applicant
KYPHON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/2008
Days to Decision
69 days
Submission Type
Summary

DISCYPHOR DIRECT CATHETER SYSTEM, DISCYPHOR DIRECT NEEDLES, LONG, DISCYPHOR DIRECT NEEDLES, REGULAR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073516
510(k) Type
Traditional
Applicant
KYPHON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/2008
Days to Decision
69 days
Submission Type
Summary