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

IBEX SPINAL SYSTEM

K Number: K091381 · Decision Aug 7, 2009
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
95
Review Days
88

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Basic Information

Device Name
IBEX SPINAL SYSTEM
K Number
K091381
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ebi, L.P.
Date Received
May 11, 2009
Decision Date
August 7, 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 Ebi, L.P.

K Number Device Name
K100438 POLARIS SPINAL SYSTEM, POLARIS/SYNERGY STRUCTURE ANTERIOR FIXATION SYSTEM
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K093880 PEANUT GROWTH CONTROL PLATING SYSTEM
K092574 ESL SPINAL SYSTEM
K093057 BIOMET VISION FOOTRING SYSTEM
K092336 C-THRU SPINAL SYSTEM
K090203 5.5 HELICAL FLANGE SPINAL SYSTEM, POLARIS COMPONENTS
K090523 POLARIS SPINAL SYSTEM
K082406 EXPANDABLE PEEK-OPTIMA IMPLANT
K082187 BIOMET ANTERIOR LUMBAR PLATE
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