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

ECLIPSE TOTAL ANKLE IMPLANT

K Number: K061749 · Decision Nov 22, 2006
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
67
Applicant Total
19
Review Days
154

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Basic Information

Device Name
ECLIPSE TOTAL ANKLE IMPLANT
K Number
K061749
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3110
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kinetikos Medical, Inc.
Date Received
June 21, 2006
Decision Date
November 22, 2006
Product Code
HSN
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
HSN Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer

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Other Clearances by Kinetikos Medical, Inc.

K Number Device Name
K061465 KMI CEMENT RESTRICTOR IMPLANT
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K041461 KMI DISTAL VOLAR RADIUS PLATE SYSTEM
K032806 KATALYST RADIAL HEAD IMPLANT
K040356 KOMPRESSOR SCREW SYSTEM
K024233 KOMPRESSOR SCREW SYSTEM
K030037 UNIVERSAL TOTAL WRIST SYSTEM
K023770 K2 HEMI TOE IMPLANT SYSTEM (FORMERLY ZOBEL GREAT TOE IMPLANT SYSTEM)
K020554 MODIFICATION TO UNIVERSAL TOTAL WRIST SYSTEM
K991873 KMI WRIST FUSION SYSTEM
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