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

NAKOMA ACP

K Number: K141993 · Decision Nov 6, 2014
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
10
Review Days
107

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Basic Information

Device Name
NAKOMA ACP
K Number
K141993
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alliance Partners, LLC
Date Received
July 22, 2014
Decision Date
November 6, 2014
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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