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

ULTIMAX DISTAL RADIAL (VOLAR) LOCKING PLATE SYSTEM

K Number: K990481 · Decision Mar 17, 1999
Classifications
1
FEI Numbers
519
Registration Numbers
519
Same Product Code
1313
Applicant Total
30
Review Days
29

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Basic Information

Device Name
ULTIMAX DISTAL RADIAL (VOLAR) LOCKING PLATE SYSTEM
K Number
K990481
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Biodynamic Technologies, Inc.
Date Received
February 16, 1999
Decision Date
March 17, 1999
Product Code
HRS
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
HRS Plate, Fixation, Bone

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Other Clearances by Biodynamic Technologies, Inc.

K Number Device Name
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K981230 ULTIMAX DISTAL FEMORAL INTRAMEDULLARY ROD SYSTEM
K980102 BTI HUMERAL INTRAMEDULLARY ROD SYSTEM
K974756 BTI LARGE (7.0MM) CANNULATED TRANSFIXING SCREWS
K972403 BTI CORTICAL BONE SCREWS
K970897 BTI DISTAL FEMORAL INTRAMEDULLARY ROD SYSTEM
K962706 EZ-FIX CANNULATED SCREW SYSTEM
K962987 EZ-FIX SMALL CANNULATED SCREW SYSTEM
K962846 EZ-FIX COMPRESSION HIP/SUPRACONDYLAR SCREW (CHS) SYSTEM
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