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

SMALL BONE FIXATION SYSTEM

K Number: K033406 · Decision Jan 15, 2004
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
10
Review Days
83

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Basic Information

Device Name
SMALL BONE FIXATION SYSTEM
K Number
K033406
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hand Innovations, Inc.
Date Received
October 24, 2003
Decision Date
January 15, 2004
Product Code
HTY
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
HTY Pin, Fixation, Smooth

Similar 510(k) Clearances

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

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Other Clearances by Hand Innovations, Inc.

K Number Device Name
K050932 DISTAL VOLAR RADIUS ANATOMICAL PLATE SYSTEM
K042059 SHOULDER FIXATION SYSTEM
K041157 MODIFICATION TO SMALL BONE FIXATION SYSTEM
K041081 FRAGMENT PLATE SYSTEM, SCREWS, PINS AND K-WIRES
K032705 DISTAL RADIUS FRACTURE REPAIR SYSTEM
K030198 HAND INNOVATIONS, INC. DISTAL RADIUS FRACTURE REPAIR SYSTEM
K023007 DISTAL RADIUS FRACTURE REPAIR SYSTEM
K013424 INTRAMEDULLARY FIXATION SYSTEM FOR THE HAND
K002775 DISTAL VOLAR RADIUS FRACTURE REPAIR SYSTEM