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

Rectangular Corpectomy Cage

K Number: K152460 · Decision Dec 22, 2015
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
276
Applicant Total
16
Review Days
116

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Basic Information

Device Name
Rectangular Corpectomy Cage
K Number
K152460
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
December 22, 2015
Product Code
MQP
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
MQP Spinal Vertebral Body Replacement Device

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