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

ELLIS EXTERNAL MINI-FIXATOR SYSTEM

K Number: K964458 · Decision Dec 9, 1996
Classifications
1
FEI Numbers
249
Registration Numbers
249
Same Product Code
403
Applicant Total
21
Review Days
32

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Basic Information

Device Name
ELLIS EXTERNAL MINI-FIXATOR SYSTEM
K Number
K964458
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Link America, Inc.
Date Received
November 7, 1996
Decision Date
December 9, 1996
Product Code
KTT
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
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

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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
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