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

GUIDE WIRES FOR CANNULATED SCREWS

K Number: K963432 · Decision Nov 13, 1996
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
56
Applicant Total
11
Review Days
75

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Basic Information

Device Name
GUIDE WIRES FOR CANNULATED SCREWS
K Number
K963432
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Orthopaedic Biosystems, Ltd.
Date Received
August 30, 1996
Decision Date
November 13, 1996
Product Code
LXT
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
LXT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite

Similar 510(k) Clearances

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

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Other Clearances by Orthopaedic Biosystems, Ltd.

K Number Device Name
K000797 OBL 2.0 MM MINI TAC ANCHOR, MODEL 10-1629-01
K982996 POLYMER OBL SB ANCHOR / SUTURE COMBINATION
K983169 POLYMER THREADED ANCHOR
K982963 POLYMER THREADED ANCHOR / SUTURE COMBINATION
K972326 PEBA ANCHOR/SUTURE COMBINATION
K963420 CANCELLOUS SCREW WASHER
K963433 THREADED FIXATION PIN
K962779 COMPRESSION SCREW
K951451 PEBA ANCHOR (MULTIPLE SIZES)
K942889 SB ANCHOR
Search all 11 clearances from Orthopaedic Biosystems, Ltd. →