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

SCAPHIX, STAPLE, FIXATION, BONE

K Number: K003033 · Decision May 30, 2001
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
230
Applicant Total
18
Review Days
244

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Basic Information

Device Name
SCAPHIX, STAPLE, FIXATION, BONE
K Number
K003033
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Avanta Orthopaedics, Inc.
Date Received
September 28, 2000
Decision Date
May 30, 2001
Product Code
JDR
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
JDR Staple, Fixation, Bone

Similar 510(k) Clearances

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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
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. →