FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Shanghai Sanyou PEEK Cage System

K Number: K163422 · Decision Sep 18, 2017
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
9
Review Days
286

Basic Information

Device Name
Shanghai Sanyou PEEK Cage System
K Number
K163422
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shanghai Sanyou Medical Co, Ltd.
Date Received
December 6, 2016
Decision Date
September 18, 2017
Product Code
ODP
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

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K Number Device Name
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K231931 Adena-Zina Spinal System
K211689 KEYSTONE PEEK Cage System
K212066 Adena-Zina System
K163366 Shanghai Sanyou CARMEN Cervical Fusion System
K152781 Adena-Zina System
K131512 KATIA SYSTEM