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

TELESCOPIC PLATE SPACER THORACOLUMBAR (TPS-TL) SPINAL SYSTEM, MODELS 8123, 8124, 8132, 8133, 8156, 8157, 8158, & 8189

K Number: K020204 · Decision Feb 21, 2002
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
276
Applicant Total
39
Review Days
30

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Basic Information

Device Name
TELESCOPIC PLATE SPACER THORACOLUMBAR (TPS-TL) SPINAL SYSTEM, MODELS 8123, 8124, 8132, 8133, 8156, 8157, 8158, & 8189
K Number
K020204
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Interpore Cross Intl.
Date Received
January 22, 2002
Decision Date
February 21, 2002
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

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Other Clearances by Interpore Cross Intl.

K Number Device Name
K050861 PEEK CAS
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K041407 TITANIUM MESH IMPLANT
K043229 MODIFICATION TO ALTIUS OCT SYSTEM
K042798 C-TEK C-TRUN ANTERIOR CERVICAL PLATE SYSTEM
K040928 EXPANDABLE PEEK VBR IMPLANT
K041794 C-TEK C-THRU ANTERIOR CERVICAL PLATE SYSTEM
K041449 SYNERGY HELICAL FLANGE PLUG, HELICAL FLANGE SEAT AND HELICAL FLANGE REDUCTION SEAT
K033961 ALTIUS OCT SYSTEM
K040168 MODIFICATION TO GEO STRUCTURE
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