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

Binary® Anterior Cervical Plate System

K Number: K192076 · Decision Aug 29, 2019
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
31
Review Days
27

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Basic Information

Device Name
Binary® Anterior Cervical Plate System
K Number
K192076
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Genesys Spine
Date Received
August 2, 2019
Decision Date
August 29, 2019
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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Other Clearances by Genesys Spine

K Number Device Name
K252322 SIros-X System
K242483 Genesys Spine AIS-C II Cervical Interbody Fusion System
K233595 Genesys Spine Sacroiliac Joint Fusion System with Navigation
K233594 Genesys Spine 3DP AIS-C II Cervical Interbody System
K220096 Genesys Spine 3DP Lumbar Interbody System
K191489 Genesys Spine 3DP Cervical Interbody System
K182987 Genesys Spine 3DP Lumbar Interbody System
K192678 Genesys Spine Binary® Lumbar Plate System
K191748 Genesys Spine Sacroiliac Joint Fusion System
K181295 Genesys Spine AIS-C Cervical Stand-Alone System
Search all 31 clearances from Genesys Spine →