FDA 510(k) Applications Submitted by JONAS WILF

FDA 510(k) Number Submission Date Device Name Applicant
K000083 01/12/2000 EBI XFIX DFS RAIL SYSTEM EBI, L.P.
K000319 02/02/2000 EBI XFIX DFS SYSTEM EBI, L.P.
K990999 03/25/1999 MODIFICATION OF: EBI SPINELINK SYSTEM ELECTRO-BIOLOGY, INC.
K001037 03/31/2000 MODIFICATION TO EBI SPINELINK SYSTEM EBI, L.P.
K991092 04/01/1999 EBI SPINELINK ANTERIOR CERVICAL SPINAL SYSTEM ELECTRO-BIOLOGY, INC.
K001357 04/28/2000 MODIFICATION TO OMEGA 21 SYSTEM EBI, L.P.
K991721 05/20/1999 EBI OMEGA 21 SYSTEM EBI ELECTRO BIOLOGY
K991941 06/09/1999 EBI XFIX DFS RAIL SYSTEM ELECTRO-BIOLOGY, INC.
K992333 07/13/1999 EBI OMEGA 21 SYSTEM ELECTRO-BIOLOGY, INC.
K992367 07/15/1999 EBI XFIX DYNAFIX SYSTEM HA COATED SCREWS ELECTRO-BIOLOGY, INC.
K982484 07/17/1998 EBI VUECATH ENDOSCOPIC SPINAL SYSTEM ELECTRO-BIOLOGY, INC.
K992515 07/28/1999 EBI XFIX DFS OPTIROM ELBOW FIXATOR EBI, L.P.
K982908 08/18/1998 MODIFICATION TO EBI SPINELINK SYSTEM ELECTRO-BIOLOGY, INC.
K992920 08/30/1999 EBI SPINELINK SYSTEM EBI, L.P.


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