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

LINK MP RECONSTRUCTION HIP

K Number: K955296 · Decision Feb 14, 1996
Classifications
1
FEI Numbers
227
Registration Numbers
227
Same Product Code
562
Applicant Total
21
Review Days
90

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Basic Information

Device Name
LINK MP RECONSTRUCTION HIP
K Number
K955296
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3350
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Link America, Inc.
Date Received
November 16, 1995
Decision Date
February 14, 1996
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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K914804 RADIUS OSTEOTOMY PLATES
K914803 SCHWABE RADIUS PLATES
K895507 LINK GIEBEL BLADE PLATE SYSTEM
K873507 LINK (R) AMERICAN-TYPE BONE STAPLE SYSTEM
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