Ace Orthopedic Manufacturing Co. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Ace Orthopedic Manufacturing Co. has 14 FDA 510(k) cleared orthopedic devices. Based in Mchenry, US.
Historical record: 14 cleared submissions from 1977 to 1994.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Mar 22, 1994
ACE HUMERAL NAIL
Orthopedic
174d
Cleared
Mar 22, 1994
AIM SUPRACONDYLAR NAIL
Orthopedic
155d
Cleared
Feb 22, 1994
ACE UNILATERAL FIXATOR II
Orthopedic
64d
Cleared
Mar 31, 1993
ACE 8.0MM CANNULATED CANCELLOUS BONE SCREW
Orthopedic
120d
Cleared
Jul 27, 1992
ACE 100 DEGREES TUBULAR PLATE
Orthopedic
159d
Cleared
Jan 12, 1982
ACE/KYLE CAPTURED HIP SCREW
Orthopedic
21d
Cleared
Mar 20, 1981
TRIPPI-WELLS DUAL PURPOSE UNIVERSAL TONG
Neurology
56d
Cleared
Sep 09, 1980
ACE FISCHER EXTERNAL FIXATION DEVICE
Orthopedic
57d
Cleared
Aug 16, 1979
ACE EXTERNAL BONE CLAMP PART #S11
Orthopedic
15d
Cleared
Nov 08, 1978
BONE CLAMP, ACE EXTERNAL
Orthopedic
12d
Cleared
Nov 08, 1978
EXTERNAL ARTICULATION
Orthopedic
12d
Cleared
Nov 08, 1978
BAR, DISTRACTION
Orthopedic
12d