Link America, Inc.
FDA 510(k) medical device clearances.
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.