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CD Horizon™ Fenestrated Screw Set, CD Horizon™ Spinal System, Kyphon™ HV-R™ Bone Cement

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201362
510(k) Type
Traditional
Applicant
Medtronic
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2020
Days to Decision
89 days
Submission Type
Summary

CD Horizon™ Fenestrated Screw Set, CD Horizon™ Spinal System, Kyphon™ HV-R™ Bone Cement

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201362
510(k) Type
Traditional
Applicant
Medtronic
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/2020
Days to Decision
89 days
Submission Type
Summary