Allo Pro Corp. - FDA 510(k) Cleared Devices
16
Total
15
Cleared
0
Denied
Allo Pro Corp. has 15 FDA 510(k) cleared orthopedic devices. Based in Mchenry, US.
Historical record: 15 cleared submissions from 1981 to 1990.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
16 devices
Cleared
Oct 22, 1990
GSB ELBOW
Orthopedic
201d
Cleared
Sep 07, 1990
SURGICAL COTTON GLOVES
General Hospital
220d
Cleared
Mar 01, 1990
CENTERING PLUG
Orthopedic
34d
Cleared
Feb 06, 1990
WEBER PERMALOCK
Orthopedic
71d
Cleared
Oct 19, 1989
BIOLOX CERAMIC BALL
Orthopedic
190d
Cleared
Jan 13, 1989
RS-CUP ACETABULAR PROSTHESIS
Orthopedic
37d
Cleared
Sep 09, 1987
KENNEDY STEM
Orthopedic
261d
Cleared
Jul 13, 1987
ZWEYMUELLER-SL HIP PROSTHESIS STEM
Orthopedic
91d
Cleared
May 28, 1985
ZWEYMULLER CUP
Orthopedic
63d
Cleared
Apr 13, 1984
WEBER-STUHMER HIP PROSTHESIS STEM
Orthopedic
10d
Cleared
Jul 12, 1983
WEBER/STIIHMER FEMORAL HEAD PROSTHESIS
Orthopedic
110d
Cleared
Apr 12, 1983
POLYETHYLENE MEDULLARY PLUG - STIIHMER/
Orthopedic
19d
Cleared
Jan 14, 1983
CEMENTLESS ZWEYMUELLER HIP ENDOPROTHES
Orthopedic
98d
Cleared
Jun 10, 1982
THE ORIGINAL LEINBACH PLATFORM TOTAL HIP
Orthopedic
83d
Cleared
Jul 27, 1981
SEMI-CONSTRAINT KEE JOINT HINGE PROSTH
Orthopedic
95d
Cleared
Jul 20, 1981
WEBER/STUEHMER HIP JOINT ENDOPROSTHESIS
Orthopedic
87d