FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

LINK DYNAMIC STAPLE

K Number: K853704 · Decision Jan 21, 1986
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
230
Applicant Total
21
Review Days
139

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Basic Information

Device Name
LINK DYNAMIC STAPLE
K Number
K853704
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Link America, Inc.
Date Received
September 4, 1985
Decision Date
January 21, 1986
Product Code
JDR
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JDR Staple, Fixation, Bone

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Other Clearances by Link America, Inc.

K Number Device Name
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
Search all 21 clearances from Link America, Inc. →