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

ORTHOPILOT 2 TOTAL HIP ARTHROPLASTY (THA) VERSION 3.0

K Number: K072899 · Decision Feb 6, 2008
Classifications
1
FEI Numbers
250
Registration Numbers
250
Same Product Code
422
Applicant Total
22
Review Days
118

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Basic Information

Device Name
ORTHOPILOT 2 TOTAL HIP ARTHROPLASTY (THA) VERSION 3.0
K Number
K072899
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aesculap Implant Systems, Inc.
Date Received
October 11, 2007
Decision Date
February 6, 2008
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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