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

PERIOGLAS PLUS - SETTABLE BONE GRAFT SUBSTITUTE

K Number: K031073 · Decision Nov 5, 2003
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
225
Applicant Total
28
Review Days
215

Basic Information

Device Name
PERIOGLAS PLUS - SETTABLE BONE GRAFT SUBSTITUTE
K Number
K031073
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
NovaBone Products, LLC
Date Received
April 4, 2003
Decision Date
November 5, 2003
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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