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

MODIFICATION TO S4 SPINAL SYSTEM

K Number: K062327 · Decision Mar 14, 2007
Classifications
1
FEI Numbers
413
Registration Numbers
413
Same Product Code
873
Applicant Total
174
Review Days
216

Basic Information

Device Name
MODIFICATION TO S4 SPINAL SYSTEM
K Number
K062327
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
AESCULAP, INC.
Date Received
August 10, 2006
Decision Date
March 14, 2007
Product Code
NKB
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
NKB Thoracolumbosacral Pedicle Screw System

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