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

Kyphon Xpede Bone Cement

K Number: K163032 · Decision Feb 27, 2017
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
107
Applicant Total
209
Review Days
119

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Basic Information

Device Name
Kyphon Xpede Bone Cement
K Number
K163032
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3027
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic, Inc.
Date Received
October 31, 2016
Decision Date
February 27, 2017
Product Code
NDN
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
NDN Cement, Bone, Vertebroplasty

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