FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

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

K Number: K201362 · Decision Aug 19, 2020
Classifications
1
FEI Numbers
80
Registration Numbers
80
Same Product Code
18
Applicant Total
33
Review Days
89

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Basic Information

Device Name
CD Horizon™ Fenestrated Screw Set, CD Horizon™ Spinal System, Kyphon™ HV-R™ Bone Cement
K Number
K201362
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3027
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic
Date Received
May 22, 2020
Decision Date
August 19, 2020
Product Code
PML
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
PML Bone Cement, Posterior Screw Augmentation

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