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

ACUFEX PATELLAR BONE BLOCK SIZER

K Number: K944500 · Decision Jun 12, 1995
Classifications
1
FEI Numbers
368
Registration Numbers
368
Same Product Code
669
Applicant Total
78
Review Days
271

Basic Information

Device Name
ACUFEX PATELLAR BONE BLOCK SIZER
K Number
K944500
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
September 14, 1994
Decision Date
June 12, 1995
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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K952535 ACUFEX ENDOBUTTON TAPE
K953276 ACUFEX TAG DELIVERY SYSTEM
K953459 ACUFEX TAG ANCHOR
K941740 ACUFEX ROTATOR CUFF FIXATION BUTTON
K951859 ACUFEX ENDOBUTTON PACK
K946346 ACUFEX TAG(R) BIOABSORBABLE ANCHORS
K941709 ACUFEX ARTHROSCOPIC DISCECTOMY SYSTEMS
Search all 78 clearances from ACUFEX MICROSURGICAL, INC. →