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

LINK SHOULDER PROSTHESIS ENDO-MODEL SYSTEM

K Number: K852365 · Decision Dec 16, 1985
Classifications
1
FEI Numbers
218
Registration Numbers
218
Same Product Code
189
Applicant Total
21
Review Days
195

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Basic Information

Device Name
LINK SHOULDER PROSTHESIS ENDO-MODEL SYSTEM
K Number
K852365
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3660
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Link America, Inc.
Date Received
June 4, 1985
Decision Date
December 16, 1985
Product Code
KWS
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
KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

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K Number Device Name
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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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