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Medtronic HV-R™ Bone Cement, Kyphon™ Xpede™ Bone Cement, CD Horizon™ Fenestrated Screw Set

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191148
510(k) Type
Traditional
Applicant
Medtronic Sofamor Danek, USA Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2019
Days to Decision
135 days
Submission Type
Summary

Medtronic HV-R™ Bone Cement, Kyphon™ Xpede™ Bone Cement, CD Horizon™ Fenestrated Screw Set

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191148
510(k) Type
Traditional
Applicant
Medtronic Sofamor Danek, USA Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2019
Days to Decision
135 days
Submission Type
Summary