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

THE MEHDIAN LUMBO-SACRAL PEDICLE SCREW SYSTEM

K Number: K973425 · Decision Feb 27, 1998
Classifications
1
FEI Numbers
326
Registration Numbers
326
Same Product Code
308
Applicant Total
57
Review Days
170

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Basic Information

Device Name
THE MEHDIAN LUMBO-SACRAL PEDICLE SCREW SYSTEM
K Number
K973425
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Corin USA
Date Received
September 10, 1997
Decision Date
February 27, 1998
Product Code
MNH
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
MNH Orthosis, Spondylolisthesis Spinal Fixation

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Other Clearances by Corin USA

K Number Device Name
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K193042 Optimized Positioning System (OPS) ReView
K192656 Optimized Positioning System (OPS) Insight
K190143 LARS AC Band Device
K190834 Corin Optimized Position System Functional Hip Analysis (OPS FHA)
K183038 Corin Optimized Positioning System (OPS) Plan
K181061 Corin Optimized Positioning System (OPS) Femoral
K152893 Corin Optimized Positioning System (OPS)
Search all 57 clearances from Corin USA →