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

Sure Lok Mini Posterior Cervical/Upper Thoracic System

K Number: K150851 · Decision Jun 4, 2015
Classifications
1
FEI Numbers
330
Registration Numbers
330
Same Product Code
429
Applicant Total
7
Review Days
65

Basic Information

Device Name
Sure Lok Mini Posterior Cervical/Upper Thoracic System
K Number
K150851
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
PRECISION SPINE, INC.
Date Received
March 31, 2015
Decision Date
June 4, 2015
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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