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

Vy Spine™ VySpan™ PCT System

K Number: K213394 · Decision Dec 10, 2021
Classifications
1
FEI Numbers
164
Registration Numbers
164
Same Product Code
117
Applicant Total
21
Review Days
56

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Basic Information

Device Name
Vy Spine™ VySpan™ PCT System
K Number
K213394
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3075
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vy Spine, LLC
Date Received
October 15, 2021
Decision Date
December 10, 2021
Product Code
NKG
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
NKG Posterior Cervical Screw System

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Other Clearances by Vy Spine, LLC

K Number Device Name
K260697 VyPlate™ Anterior Cervical Plate System
K253432 DiversiVy™ Facet Screw System
K253158 VyBrate™ VBR System
K241783 FortiVy™ OsteoVy™ Lumbar IBF
K242784 Vy Spine™ VyLam™ Laminoplasty System
K233807 LumiVy™ Lumbar IBF System
K231836 ClariVy™ Cervical IBF System
K231744 VyLink™ Spinal Screw System
K232471 Vy Spine™ VyLam™ Laminoplasty System
K232167 VySpan™ PCT System
Search all 21 clearances from Vy Spine, LLC →