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

CAPSURE(R) PS SYSTEM

K Number: K122233 · Decision Oct 11, 2012
Classifications
1
FEI Numbers
342
Registration Numbers
342
Same Product Code
302
Applicant Total
59
Review Days
77

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Basic Information

Device Name
CAPSURE(R) PS SYSTEM
K Number
K122233
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spine Wave, Inc.
Date Received
July 26, 2012
Decision Date
October 11, 2012
Product Code
MNI
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
MNI Orthosis, Spinal Pedicle Fixation

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