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

AVANTA ORTHOPAEDICS TRAPEZIAL IMPLANT

K Number: K964381 · Decision Jan 22, 1997
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
25
Applicant Total
18
Review Days
79

Basic Information

Device Name
AVANTA ORTHOPAEDICS TRAPEZIAL IMPLANT
K Number
K964381
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3770
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
AVANTA ORTHOPAEDICS, INC.
Date Received
November 4, 1996
Decision Date
January 22, 1997
Product Code
KYI
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
KYI Prosthesis, Wrist, Carpal Trapezium

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Other Clearances by AVANTA ORTHOPAEDICS, INC.

K Number Device Name
K030881 AVANTA CARPAL FUSION PLATING SYSTEM
K021859 WRIST IMPLANT
K023604 MODIFICATION TO RADIAL HEAD IMPLANT
K013629 FINGER JOINT PROSTHESIS
K010847 K'FIX
K011819 RADIAL HEAD IMPLANT
K003033 SCAPHIX, STAPLE, FIXATION, BONE
K010786 ULNAR HEAD IMPLANT
K002644 RADIAL HEAD IMPLANT
K990596 DISTAL RADIUS FRACTURE FIXATION PLATE SYSTEM
Search all 18 clearances from AVANTA ORTHOPAEDICS, INC. →