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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