Acufex Microsurgical, Inc. - FDA 510(k) Cleared Devices
78
Total
75
Cleared
0
Denied
Acufex Microsurgical, Inc. has 75 FDA 510(k) cleared orthopedic devices. Based in Mchenry, US.
Historical record: 75 cleared submissions from 1980 to 1996.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
78 devices
Cleared
Jul 10, 1996
ACUFEX TAG BIOABSORBABLE ANCHORS
Orthopedic
79d
Cleared
Jun 21, 1996
PROLINE FAST PASS ARTHOSCOPIC NEEDLE PASSER
General & Plastic Surgery
38d
Cleared
Feb 15, 1996
ACUFEX ENDOFIX ABSORBABLE INTERFERENCE SCREW
Orthopedic
157d
Cleared
Feb 08, 1996
ACUFEX ENDOBUTTON TAPE
General & Plastic Surgery
252d
Cleared
Oct 05, 1995
ACUFEX TAG DELIVERY SYSTEM
Orthopedic
83d
Cleared
Aug 23, 1995
ACUFEX TAG ANCHOR
Orthopedic
30d
Cleared
Jun 30, 1995
ACUFEX ROTATOR CUFF FIXATION BUTTON
General & Plastic Surgery
449d
Cleared
Jun 12, 1995
ACUFEX PATELLAR BONE BLOCK SIZER
Orthopedic
271d
Cleared
Jun 09, 1995
ACUFEX ENDOBUTTON PACK
Orthopedic
49d
Cleared
Apr 26, 1995
ACUFEX TAG(R) BIOABSORBABLE ANCHORS
Orthopedic
117d
Cleared
Apr 14, 1995
ACUFEX ARTHROSCOPIC DISCECTOMY SYSTEMS
Orthopedic
373d
Cleared
Mar 20, 1995
BIOABSORBABLE INTERFERENCE SCREW
Orthopedic
242d
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