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

EBI ACUMEN SURGICAL NAVIGATION SYSTEM

K Number: K031732 · Decision Oct 15, 2003
Classifications
1
FEI Numbers
250
Registration Numbers
250
Same Product Code
422
Applicant Total
95
Review Days
133

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Basic Information

Device Name
EBI ACUMEN SURGICAL NAVIGATION SYSTEM
K Number
K031732
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ebi, L.P.
Date Received
June 4, 2003
Decision Date
October 15, 2003
Product Code
HAW
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HAW Neurological Stereotaxic Instrument

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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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