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

SPECTRUM CERVICAL SPINAL SYSTEM

K Number: K022997 · Decision Dec 6, 2002
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
4
Review Days
88

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Basic Information

Device Name
SPECTRUM CERVICAL SPINAL SYSTEM
K Number
K022997
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spinal Innovations, LLC
Date Received
September 9, 2002
Decision Date
December 6, 2002
Product Code
KWQ
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

Similar 510(k) Clearances

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

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Other Clearances by Spinal Innovations, LLC

K Number Device Name
K013196 ASCEND SPINAL FIXATION SYSTEM WITH THE SHADOW SPINAL SYSTEM
K010639 CONVERGENCE CERVICAL SPINAL SYSTEM
K002069 ASCEND SPINAL FIXATION SYSTEM