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

ULNAR HEAD IMPLANT

K Number: K010786 · Decision Apr 11, 2001
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
15
Applicant Total
18
Review Days
27

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Basic Information

Device Name
ULNAR HEAD IMPLANT
K Number
K010786
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3810
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Avanta Orthopaedics, Inc.
Date Received
March 15, 2001
Decision Date
April 11, 2001
Product Code
KXE
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
KXE Prosthesis, Wrist, Hemi-, Ulnar

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KXE), 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
K013629 FINGER JOINT PROSTHESIS
K010847 K'FIX
K011819 RADIAL HEAD IMPLANT
K003033 SCAPHIX, STAPLE, FIXATION, BONE
K002644 RADIAL HEAD IMPLANT
K990596 DISTAL RADIUS FRACTURE FIXATION PLATE SYSTEM
K982268 ULNAR HEAD IMPLANT
Search all 18 clearances from Avanta Orthopaedics, Inc. →