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

UNI-T SPINAL SYSTEM

K Number: K013301 · Decision Feb 13, 2002
Classifications
1
FEI Numbers
342
Registration Numbers
342
Same Product Code
302
Applicant Total
12
Review Days
133

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Basic Information

Device Name
UNI-T SPINAL SYSTEM
K Number
K013301
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spine Vision, Inc.
Date Received
October 3, 2001
Decision Date
February 13, 2002
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MNI), ordered by most recent decision date.

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Other Clearances by Spine Vision, Inc.

K Number Device Name
K052406 UNI-THREAD SPINAL SYSTEM
K030526 PEDIGUARD NERVE DETECTOR SYSTEM
K042930 SPACEVISION CAGE SYSTEM
K042640 UNI-THREAD SPINAL SYSTEM
K033508 PLUS PIVOT LINK UNIVERSAL SYSTEM
K032398 PLUS PIVOT LINK UNIVERSAL SYSTEM
K022271 PLUS PIVOT LINK UNIVERSAL SYSTEM
K021507 PLUS PIVOT LINK UNIVERSAL SYSTEM
K021510 UNI-T UNI-THREAD SPINAL SYSTEM
K013312 P.L.U.S. SYSTEM (PIVOT LINK UNIVERSAL SYSTEM)
Search all 12 clearances from Spine Vision, Inc. →