Link America, Inc.
Link America, Inc. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 1997.
Top product codes for Link America, Inc.
Recent clearances by Link America, Inc.
- K972760 — LINK, ACETABULAR REVISION MESH CUP
- K964458 — ELLIS EXTERNAL MINI-FIXATOR SYSTEM
- K955296 — LINK MP RECONSTRUCTION HIP
- K954186 — SLED UNICOMPARTMENT KNEE SYSTEM
- K931571 — LINK CERAMIC HEADS 12/14 X 32MM
- K931572 — LINK CERAMIC HEADS 14/16 X 32MM
- K920756 — FELDMUHLE CERAMIC HEAD
- K914804 — RADIUS OSTEOTOMY PLATES
- K914803 — SCHWABE RADIUS PLATES
- K895507 — LINK GIEBEL BLADE PLATE SYSTEM
- K873507 — LINK (R) AMERICAN-TYPE BONE STAPLE SYSTEM
- K871535 — SMILJANIC BONE REPOSITIONING FORCEPS
- K854935 — LINK METAL-BACKED ACETABULAR CUPS
- K854465 — LINK CONTOUR RIBBED HIP PROSTHESES SYSTEM
- K853704 — LINK DYNAMIC STAPLE
- K854825 — LINK SMALL BONE PLATES
- K854826 — LINK CANCELLOUS SCREWS
- K854827 — LINK CORTICAL SCREWS
- K852365 — LINK SHOULDER PROSTHESIS ENDO-MODEL SYSTEM
- K852369 — LIDGRER-LUND ACETABULAR SOCKETS
- K840423 — HARRINGTON-TYPE INSTRU-SCOLIOSIS
Data sourced from openFDA. This site is unofficial and independent of the FDA.