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

ULTIMAX CORTICAL BONE SCREWS

K Number: K990513 · Decision Mar 17, 1999
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
30
Review Days
27

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ULTIMAX CORTICAL BONE SCREWS
K Number
K990513
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Biodynamic Technologies, Inc.
Date Received
February 18, 1999
Decision Date
March 17, 1999
Product Code
HWC
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
HWC Screw, Fixation, Bone

Similar 510(k) Clearances

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

View all

Other Clearances by Biodynamic Technologies, Inc.

K Number Device Name
K990436 ULTIMAX TROCHANTERIC INTRAMEDULLARY ROD SYSTEM
K990481 ULTIMAX DISTAL RADIAL (VOLAR) LOCKING PLATE SYSTEM
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
Search all 30 clearances from Biodynamic Technologies, Inc. →