Link America, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
21
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K972760LINK, ACETABULAR REVISION MESH CUPOctober 22, 1997
K964458ELLIS EXTERNAL MINI-FIXATOR SYSTEMDecember 9, 1996
K955296LINK MP RECONSTRUCTION HIPFebruary 14, 1996
K954186SLED UNICOMPARTMENT KNEE SYSTEMJanuary 26, 1996
K931571LINK CERAMIC HEADS 12/14 X 32MMApril 19, 1994
K931572LINK CERAMIC HEADS 14/16 X 32MMMarch 28, 1994
K920756FELDMUHLE CERAMIC HEADMay 18, 1992
K914804RADIUS OSTEOTOMY PLATESApril 29, 1992
K914803SCHWABE RADIUS PLATESApril 28, 1992
K895507LINK GIEBEL BLADE PLATE SYSTEMMarch 13, 1990
K873507LINK (R) AMERICAN-TYPE BONE STAPLE SYSTEMSeptember 16, 1987
K871535SMILJANIC BONE REPOSITIONING FORCEPSMay 14, 1987
K854935LINK METAL-BACKED ACETABULAR CUPSMarch 5, 1986
K854465LINK CONTOUR RIBBED HIP PROSTHESES SYSTEMFebruary 10, 1986
K854825LINK SMALL BONE PLATESJanuary 21, 1986
K853704LINK DYNAMIC STAPLEJanuary 21, 1986
K854826LINK CANCELLOUS SCREWSDecember 27, 1985
K854827LINK CORTICAL SCREWSDecember 27, 1985
K852365LINK SHOULDER PROSTHESIS ENDO-MODEL SYSTEMDecember 16, 1985
K852369LIDGRER-LUND ACETABULAR SOCKETSJune 18, 1985