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

XPS 3000 SYSTEM

K Number: K010677 · Decision May 7, 2001
Classifications
1
FEI Numbers
368
Registration Numbers
368
Same Product Code
669
Applicant Total
28
Review Days
61

Basic Information

Device Name
XPS 3000 SYSTEM
K Number
K010677
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MEDTRONIC XOMED, INC.
Date Received
March 7, 2001
Decision Date
May 7, 2001
Product Code
HRX
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
HRX Arthroscope

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