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

Amendia Cervical Plate System

K Number: K152455 · Decision Oct 15, 2015
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
16
Review Days
48

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Basic Information

Device Name
Amendia Cervical Plate System
K Number
K152455
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Amendia, Inc.
Date Received
August 28, 2015
Decision Date
October 15, 2015
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 Amendia, Inc.

K Number Device Name
K160924 Amendia Interbody Fusion Devices
K161842 Overwatch Spine System
K152920 Savannah-T® Pedicle Screw System
K153152 Syzygy Stabilization System
K160291 Optimus ALIF System
K152972 Amendia Stand-Alone Cervical System
K151310 Amendia Interbody Fusion Devices
K152460 Rectangular Corpectomy Cage
K151322 Amendia Interbody Fusion Devices
K150395 Omega LIF System
Search all 16 clearances from Amendia, Inc. →