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

KATALYST RADIAL HEAD IMPLANT

K Number: K032806 · Decision Apr 16, 2004
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
32
Applicant Total
19
Review Days
220

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Basic Information

Device Name
KATALYST RADIAL HEAD IMPLANT
K Number
K032806
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3170
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kinetikos Medical, Inc.
Date Received
September 9, 2003
Decision Date
April 16, 2004
Product Code
KWI
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
KWI Prosthesis, Elbow, Hemi-, Radial, Polymer

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Other Clearances by Kinetikos Medical, Inc.

K Number Device Name
K061749 ECLIPSE TOTAL ANKLE IMPLANT
K061465 KMI CEMENT RESTRICTOR IMPLANT
K051611 MBARESORB IMPLANT
K041461 KMI DISTAL VOLAR RADIUS PLATE SYSTEM
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
Search all 19 clearances from Kinetikos Medical, Inc. →