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FDA 510(k) Applications Submitted by BUCKMAN CO., INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K950099
01/10/1995
SYNERGY(TM) TI POSTERIOR SPINAL SYSTEM
BUCKMAN CO., INC.
K960451
01/30/1996
WEBB-MORLEY SPINE SYSTEM
BUCKMAN CO., INC.
K950999
03/03/1995
KSF POSTERIOR SPINGAL FIXATOR FOR SEVERE SPONDYLOLISTHESIS
BUCKMAN CO., INC.
K961320
04/05/1996
CROSS MEDICAL BONE PLATE SYSTEM/ CM BONE PLATE SYSTEM/CROSS TI BONE PLATE SYSTEM
BUCKMAN CO., INC.
K964252
10/24/1996
ORTHOCHUCK
BUCKMAN CO., INC.
K974641
12/15/1997
FUTURELASE 3000/3002 ERBIUM LASER SYSTEM
BUCKMAN CO., INC.
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