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

SPACEVISION CAGE SYSTEM

K Number: K042930 · Decision Dec 28, 2004
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
276
Applicant Total
12
Review Days
67

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Basic Information

Device Name
SPACEVISION CAGE SYSTEM
K Number
K042930
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spine Vision, Inc.
Date Received
October 22, 2004
Decision Date
December 28, 2004
Product Code
MQP
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
MQP Spinal Vertebral Body Replacement Device

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MQP), 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
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
K013301 UNI-T SPINAL SYSTEM
K013312 P.L.U.S. SYSTEM (PIVOT LINK UNIVERSAL SYSTEM)
Search all 12 clearances from Spine Vision, Inc. →