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

MODIFICATION TO LDR SPINE ROI INTERBODY FUSION SYSTEM; ROI-A IMPLANT SYSTEM

K Number: K090507 · Decision Jun 25, 2009
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
25
Review Days
120

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Basic Information

Device Name
MODIFICATION TO LDR SPINE ROI INTERBODY FUSION SYSTEM; ROI-A IMPLANT SYSTEM
K Number
K090507
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ldr Spine USA
Date Received
February 25, 2009
Decision Date
June 25, 2009
Product Code
MAX
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

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Other Clearances by Ldr Spine USA

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K150765 LDR Spine ROI-C Cervical Cage System
K110327 LDR SPINE ROI-A INTERBODY FUSION SYSTEM
K102331 LDR SPINE USA SPINETUNE TL SPINAL SYSTEM
K102265 LDR SPINE USA C-PLATE, TL ANTERIOR CERVICAL PLATE SYSTEM
K100575 LDR SPINE USA SPINE TUNE TL SPINE SYSTEM
K091088 LDR SPINE CERVICAL INTERBODY FUSION SYSTEM
K083857 LDR SPINE ROI-C IMPLANT
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