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

K2 HEMI TOE IMPLANT SYSTEM (FORMERLY ZOBEL GREAT TOE IMPLANT SYSTEM)

K Number: K023770 · Decision Dec 12, 2002
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
45
Applicant Total
19
Review Days
30

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Basic Information

Device Name
K2 HEMI TOE IMPLANT SYSTEM (FORMERLY ZOBEL GREAT TOE IMPLANT SYSTEM)
K Number
K023770
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3730
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kinetikos Medical, Inc.
Date Received
November 12, 2002
Decision Date
December 12, 2002
Product Code
KWD
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
KWD Prosthesis, Toe, Hemi-, Phalangeal

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Other Clearances by Kinetikos Medical, Inc.

K Number Device Name
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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
K020554 MODIFICATION TO UNIVERSAL TOTAL WRIST SYSTEM
K991873 KMI WRIST FUSION SYSTEM
Search all 19 clearances from Kinetikos Medical, Inc. →