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

LINK CONTOUR RIBBED HIP PROSTHESES SYSTEM

K Number: K854465 · Decision Feb 10, 1986
Classifications
1
FEI Numbers
227
Registration Numbers
227
Same Product Code
562
Applicant Total
21
Review Days
96

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Basic Information

Device Name
LINK CONTOUR RIBBED HIP PROSTHESES SYSTEM
K Number
K854465
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3350
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Link America, Inc.
Date Received
November 6, 1985
Decision Date
February 10, 1986
Product Code
JDI
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
JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

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K Number Device Name
K972760 LINK, ACETABULAR REVISION MESH CUP
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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
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