FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

OSTEOMILL BONE GRINDER

K Number: K861164 · Decision May 2, 1986
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
3
Applicant Total
30
Review Days
35

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Basic Information

Device Name
OSTEOMILL BONE GRINDER
K Number
K861164
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Biodynamic Technologies, Inc.
Date Received
March 28, 1986
Decision Date
May 2, 1986
Product Code
LYS
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
LYS Bone Mill

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Other Clearances by Biodynamic Technologies, Inc.

K Number Device Name
K990436 ULTIMAX TROCHANTERIC INTRAMEDULLARY ROD SYSTEM
K990481 ULTIMAX DISTAL RADIAL (VOLAR) LOCKING PLATE SYSTEM
K990513 ULTIMAX CORTICAL BONE SCREWS
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
Search all 30 clearances from Biodynamic Technologies, Inc. →