Last synced on 25 November 2022 at 11:04 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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