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

HEALOS II BONE GRAFT SUBSTITUTE

K Number: K081432 · Decision Aug 29, 2008
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
229
Applicant Total
68
Review Days
100

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Basic Information

Device Name
HEALOS II BONE GRAFT SUBSTITUTE
K Number
K081432
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Depuy Spine, Inc.
Date Received
May 21, 2008
Decision Date
August 29, 2008
Product Code
LYC
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
LYC Bone Grafting Material, Synthetic

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K Number Device Name
K201831 CONFIDENCE Spinal Cement System
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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
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