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

SEEPLATE CERVICAL PLATE SYSTEM

K Number: K082037 · Decision Sep 26, 2008
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
16
Review Days
71

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Basic Information

Device Name
SEEPLATE CERVICAL PLATE SYSTEM
K Number
K082037
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Amedica Corp.
Date Received
July 17, 2008
Decision Date
September 26, 2008
Product Code
KWQ
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

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K Number Device Name
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K142347 Amedica Valeo II Interbody Fusion Device
K121892 PHANTOM PLUS CERAMIC CAGE SYSTEM
K091278 VALEO SPACER SYSTEM
K073430 VALEO PEDICLE SCREW SPINAL SYSTEM
K073505 MODIFICATION TO VALEO VBR
K073125 VALEO VBR
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