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

CONFIDENCE Spinal Cement System

K Number: K201831 · Decision Aug 31, 2020
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
107
Applicant Total
68
Review Days
60

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Basic Information

Device Name
CONFIDENCE Spinal Cement System
K Number
K201831
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3027
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Depuy Spine, Inc.
Date Received
July 2, 2020
Decision Date
August 31, 2020
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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Other Clearances by Depuy Spine, Inc.

K Number Device Name
K142185 EXPEDIUM VERSE SPINE SYSTEM
K111136 EXPEDIUM SPINE SYSTEM, VIPER SYSTEM, VIPER 2 SYSTEM
K121020 VIPER SYSTEM
K110353 MOUNTAINEER OCT SPINAL SYSTEM
K110216 EXPEDIUM SYSTEM, VIPER SYSTEM
K103133 VEPER SYSTEM, EXPEDIUM SYSTEM
K101993 VIPER SYSTEM, EXPEDIUM SYSTEM
K103100 MOUNTAINEER OCT SPINAL SYSTEM
K101762 VIPER F2 FACET FIXATION SYSTEM
K102701 VIPER SPINE SYSTEM
Search all 68 clearances from Depuy Spine, Inc. →