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

ENDOSKELETON TA VERTEBRAL BODY REPLACEMENT

K Number: K032812 · Decision Dec 8, 2003
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
276
Applicant Total
23
Review Days
90

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Basic Information

Device Name
ENDOSKELETON TA VERTEBRAL BODY REPLACEMENT
K Number
K032812
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Orthovita, Inc.
Date Received
September 9, 2003
Decision Date
December 8, 2003
Product Code
MQP
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
MQP Spinal Vertebral Body Replacement Device

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K103173 VITOSS BA BIMODAL BIOACTIVE BONE GRAFT SUBSTITUTE
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K102545 FM-02 BONE GRAFT SUBSTITUTE
K091618 VITOMATRIX
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