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

ACUFEX(R) ARTHROPLASTY INSTRUMENTS

K Number: K940985 · Decision May 16, 1994
Classifications
1
FEI Numbers
368
Registration Numbers
368
Same Product Code
669
Applicant Total
78
Review Days
76

Basic Information

Device Name
ACUFEX(R) ARTHROPLASTY INSTRUMENTS
K Number
K940985
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
ACUFEX MICROSURGICAL, INC.
Date Received
March 1, 1994
Decision Date
May 16, 1994
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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