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

VALEO CERVICAL PLATE SYSTEM

K Number: K071990 · Decision Oct 29, 2007
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
16
Review Days
101

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Basic Information

Device Name
VALEO CERVICAL PLATE SYSTEM
K Number
K071990
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Amedica Corp.
Date Received
July 20, 2007
Decision Date
October 29, 2007
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KWQ), ordered by most recent decision date.

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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
K142264 Valeo C Spacer System, Valeo II C IBF Device
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
Search all 16 clearances from Amedica Corp. →