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

FINGER JOINT PROSTHESIS

K Number: K013629 · Decision Jan 25, 2002
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
13
Applicant Total
18
Review Days
81

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Basic Information

Device Name
FINGER JOINT PROSTHESIS
K Number
K013629
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3230
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Avanta Orthopaedics, Inc.
Date Received
November 5, 2001
Decision Date
January 25, 2002
Product Code
KYJ
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
KYJ Prosthesis, Finger, Constrained, Polymer

Similar 510(k) Clearances

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

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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
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
K982268 ULNAR HEAD IMPLANT
Search all 18 clearances from Avanta Orthopaedics, Inc. →