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

UNIVERSAL TOTAL WRIST SYSTEM

K Number: K030037 · Decision Feb 5, 2003
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
16
Applicant Total
19
Review Days
30

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Basic Information

Device Name
UNIVERSAL TOTAL WRIST SYSTEM
K Number
K030037
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3800
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kinetikos Medical, Inc.
Date Received
January 6, 2003
Decision Date
February 5, 2003
Product Code
JWJ
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
JWJ Prosthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JWJ), ordered by most recent decision date.

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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
K032806 KATALYST RADIAL HEAD IMPLANT
K040356 KOMPRESSOR SCREW SYSTEM
K024233 KOMPRESSOR SCREW 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. →