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

VU E*POD VERTEBRAL BODY REPLACEMENT

K Number: K071031 · Decision Jul 30, 2007
Classifications
1
FEI Numbers
215
Registration Numbers
215
Same Product Code
275
Applicant Total
20
Review Days
110

Basic Information

Device Name
VU E*POD VERTEBRAL BODY REPLACEMENT
K Number
K071031
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
THEKEN SPINE LLC
Date Received
April 11, 2007
Decision Date
July 30, 2007
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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K Number Device Name
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K102323 CERVICAL STANDALONE INTERVERTEBRAL BODY FUSION DEVICE
K101310 VU APOD INTERVERTEBRAL BODY FUSION DEVICE
K100970 STAINLESS STEEL SPINAL SYSTEM
K091266 THEKEN CORAL SPINAL SYSTEM
K083863 THEKEN ATOLL OCT SPINAL SYSTEM
K083073 THEKEN ATOLL CERVICO-THORACIC SYSTEM
K082712 THEKEN SPINE VU EPOD AND VU LPOD SYSTEM
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