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

VITOMATRIX

K Number: K091618 · Decision Sep 27, 2010
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
229
Applicant Total
23
Review Days
481

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Basic Information

Device Name
VITOMATRIX
K Number
K091618
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Orthovita, Inc.
Date Received
June 3, 2009
Decision Date
September 27, 2010
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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Other Clearances by Orthovita, Inc.

K Number Device Name
K163621 Vitoss Bioactive (BA) Injectable
K161447 HydroSet XT
K153608 Vitoss BiModal Bone Graft Substitute Foam Strip
K153306 Imbibe Needle
K140868 STRYKER KWIC NEEDLE
K140414 IMBIBE NEEDLE
K103173 VITOSS BA BIMODAL BIOACTIVE BONE GRAFT SUBSTITUTE
K101171 ORTHOVITA PEEK SPACER
K102545 FM-02 BONE GRAFT SUBSTITUTE
K080108 CORTOSS BONE AUGMENTATION MATERIAL
Search all 23 clearances from Orthovita, Inc. →