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

ZODIAC POLYAXIAL SPINAL FIXATION SYSTEM

K Number: K100685 · Decision Jun 18, 2010
Classifications
1
FEI Numbers
330
Registration Numbers
330
Same Product Code
429
Applicant Total
34
Review Days
100

Basic Information

Device Name
ZODIAC POLYAXIAL SPINAL FIXATION SYSTEM
K Number
K100685
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ALPHATEC SPINE, INC.
Date Received
March 10, 2010
Decision Date
June 18, 2010
Product Code
KWP
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
KWP Appliance, Fixation, Spinal Interlaminal

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