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

Valeo C Spacer System, Valeo II C IBF Device

K Number: K142264 · Decision Dec 8, 2014
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
16
Review Days
115

Basic Information

Device Name
Valeo C Spacer System, Valeo II C IBF Device
K Number
K142264
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Amedica Corp.
Date Received
August 15, 2014
Decision Date
December 8, 2014
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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Other Clearances by Amedica Corp.

K Number Device Name
K173453 Valeo® C+CSC with Lumen Interbody Fusion Device
K161405 Valeo II Interbody Fusion Device System
K143518 Valeo Spacer System and Valeo II Interbody Fusion Device System
K142347 Amedica Valeo II Interbody Fusion Device
K121892 PHANTOM PLUS CERAMIC CAGE SYSTEM
K091278 VALEO SPACER SYSTEM
K082037 SEEPLATE CERVICAL PLATE SYSTEM
K073430 VALEO PEDICLE SCREW SPINAL SYSTEM
K073505 MODIFICATION TO VALEO VBR
K073125 VALEO VBR
Search all 16 clearances from Amedica Corp. →