Instrument Makar, Inc. - FDA 510(k) Cleared Devices
28
Total
27
Cleared
0
Denied
Instrument Makar, Inc. has 27 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 27 cleared submissions from 1979 to 2000. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Instrument Makar, Inc. Filter by specialty or product code using the sidebar.
28 devices
Cleared
Nov 15, 2000
LITWIN CRUICATE ANCHOR
Orthopedic
86d
Cleared
Nov 06, 1998
ST LEGER CEMENTED SEMI-CONSTRAINED TOTAL KNEE IMPLANT
Orthopedic
233d
Cleared
May 06, 1997
BIOSPHERE SUTURE ANCHOR
Orthopedic
251d
Cleared
Feb 25, 1997
DISPOSABLE APRON
General Hospital
116d
Cleared
Nov 19, 1996
FLUID BARRIER BOOT KNEE & ANKLE-HIGH
General Hospital
329d
Cleared
Jul 09, 1996
BIOASBSORBABLE MINI-SCREW SUTURE ANCHOR
Orthopedic
151d
Cleared
Jul 31, 1995
BIOABSORBABLE INTERFERENCE SCREW
Orthopedic
390d
Cleared
Feb 23, 1995
MAKAR FULL AND HALF FACE SHIELD
General Hospital
254d
Cleared
Feb 23, 1995
LAPRASCOPIC GRASPER
Gastroenterology & Urology
188d
Cleared
Feb 10, 1994
INSTRUMENT MAKAR PERFIX INTERFERENCE BONE SCREW
Orthopedic
350d
Cleared
Oct 27, 1993
BONE SCREWS
Orthopedic
453d
Cleared
Nov 22, 1991
MAKAR MINI CANNULATED CANCELLOUS SCREWS
Orthopedic
199d