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

MODIFICATION TO ISOBAR SPINAL SYSTEM

K Number: K020245 · Decision Feb 1, 2002
Classifications
1
FEI Numbers
326
Registration Numbers
326
Same Product Code
308
Applicant Total
8
Review Days
8

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Basic Information

Device Name
MODIFICATION TO ISOBAR SPINAL SYSTEM
K Number
K020245
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Scien'Tx USA, Inc.
Date Received
January 24, 2002
Decision Date
February 1, 2002
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

Similar 510(k) Clearances

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

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Other Clearances by Scien'Tx USA, Inc.

K Number Device Name
K013447 ISOBAR SPINAL SYSTEM
K013439 ANTERIOR CERVICAL PLATE SYSTEM
K013444 ISOBAR SPINAL SYSTEM
K013440 ISOBAR SPINAL SYSTEM
K991326 ISOBAR SEMI-RIGID SPINAL SYSTEM
K990721 ISOLOCK SPINAL SYSTEM
K990118 ISOBAR SPINAL SYSTEM