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

EBI SPINELINK - II SPINAL FIXATION SYSTEM

K Number: K012516 · Decision Nov 27, 2001
Classifications
1
FEI Numbers
321
Registration Numbers
321
Same Product Code
429
Applicant Total
95
Review Days
113

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Basic Information

Device Name
EBI SPINELINK - II SPINAL FIXATION SYSTEM
K Number
K012516
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3050
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ebi, L.P.
Date Received
August 6, 2001
Decision Date
November 27, 2001
Product Code
KWP
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
KWP Appliance, Fixation, Spinal Interlaminal

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Other Clearances by Ebi, L.P.

K Number Device Name
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K093880 PEANUT GROWTH CONTROL PLATING SYSTEM
K092574 ESL SPINAL SYSTEM
K093057 BIOMET VISION FOOTRING SYSTEM
K092336 C-THRU SPINAL SYSTEM
K091381 IBEX SPINAL SYSTEM
K090203 5.5 HELICAL FLANGE SPINAL SYSTEM, POLARIS COMPONENTS
K090523 POLARIS SPINAL SYSTEM
K082406 EXPANDABLE PEEK-OPTIMA IMPLANT
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