Link America, Inc. - FDA 510(k) Cleared Devices
21
Total
19
Cleared
0
Denied
Link America, Inc. has 19 FDA 510(k) cleared orthopedic devices. Based in Mchenry, US.
Historical record: 19 cleared submissions from 1984 to 1997.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
21 devices
Cleared
Oct 22, 1997
LINK, ACETABULAR REVISION MESH CUP
Orthopedic
90d
Cleared
Dec 09, 1996
ELLIS EXTERNAL MINI-FIXATOR SYSTEM
Orthopedic
32d
Cleared
Feb 14, 1996
LINK MP RECONSTRUCTION HIP
Orthopedic
90d
Cleared
Jan 26, 1996
SLED UNICOMPARTMENT KNEE SYSTEM
Orthopedic
142d
Cleared
Apr 19, 1994
LINK CERAMIC HEADS 12/14 X 32MM
Orthopedic
385d
Cleared
Mar 28, 1994
LINK CERAMIC HEADS 14/16 X 32MM
Orthopedic
363d
Cleared
May 18, 1992
FELDMUHLE CERAMIC HEAD
Orthopedic
89d
Cleared
Apr 29, 1992
RADIUS OSTEOTOMY PLATES
Orthopedic
188d
Cleared
Apr 28, 1992
SCHWABE RADIUS PLATES
Orthopedic
187d
Cleared
Mar 13, 1990
LINK GIEBEL BLADE PLATE SYSTEM
Orthopedic
183d
Cleared
Sep 16, 1987
LINK (R) AMERICAN-TYPE BONE STAPLE SYSTEM
Orthopedic
16d
Cleared
May 14, 1987
SMILJANIC BONE REPOSITIONING FORCEPS
General & Plastic Surgery
24d
Cleared
Mar 05, 1986
LINK METAL-BACKED ACETABULAR CUPS
Orthopedic
85d
Cleared
Feb 10, 1986
LINK CONTOUR RIBBED HIP PROSTHESES SYSTEM
Orthopedic
96d
Cleared
Jan 21, 1986
LINK DYNAMIC STAPLE
Orthopedic
139d
Cleared
Jan 21, 1986
LINK SMALL BONE PLATES
Orthopedic
49d
Cleared
Dec 27, 1985
LINK CANCELLOUS SCREWS
Orthopedic
24d
Cleared
Dec 27, 1985
LINK CORTICAL SCREWS
Orthopedic
24d
Cleared
Dec 16, 1985
LINK SHOULDER PROSTHESIS ENDO-MODEL SYSTEM
Orthopedic
195d
Cleared
Jun 18, 1985
LIDGRER-LUND ACETABULAR SOCKETS
Orthopedic
14d
Cleared
Mar 23, 1984
HARRINGTON-TYPE INSTRU-SCOLIOSIS
Orthopedic
52d