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

Mineral Collagen Composite Bioactive Moldable

K Number: K182074 · Decision Mar 21, 2019
Classifications
1
FEI Numbers
229
Registration Numbers
229
Same Product Code
491
Applicant Total
47
Review Days
232

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Basic Information

Device Name
Mineral Collagen Composite Bioactive Moldable
K Number
K182074
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3045
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Collagen Matrix, Inc.
Date Received
August 1, 2018
Decision Date
March 21, 2019
Product Code
MQV
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
MQV Filler, Bone Void, Calcium Compound

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K233203 Soft Tissue Augmentation Resorbable Matrix
K240424 Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix
K231942 Mineral Collagen Composite Bioactive Extra Moldable
K221735 Mineral Collagen Composite Bioactive Moldable
K213341 Fibrillar Collagen Wound Dressing
K202183 Porcine Mineral Collagen Composite
K201859 Porcine Mineral Collagen Composite Moldable
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