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

UNI-THREAD SPINAL SYSTEM

K Number: K042640 · Decision Nov 23, 2004
Classifications
1
FEI Numbers
338
Registration Numbers
338
Same Product Code
308
Applicant Total
8
Review Days
57

Basic Information

Device Name
UNI-THREAD SPINAL SYSTEM
K Number
K042640
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SPINEVISION, INC.
Date Received
September 27, 2004
Decision Date
November 23, 2004
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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K022271 PLUS PIVOT LINK UNIVERSAL SYSTEM
K013312 P.L.U.S. SYSTEM (PIVOT LINK UNIVERSAL SYSTEM)
K013301 UNI-T SPINAL SYSTEM