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FDA 510(k) Applications Submitted by WENDY SPIELBERGER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K040168
01/26/2004
MODIFICATION TO GEO STRUCTURE
INTERPORE CROSS INTL.
K050861
04/05/2005
PEEK CAS
INTERPORE CROSS INTL.
K040928
04/09/2004
EXPANDABLE PEEK VBR IMPLANT
INTERPORE CROSS INTL.
K041407
05/27/2004
TITANIUM MESH IMPLANT
INTERPORE CROSS INTL.
K041449
06/01/2004
SYNERGY HELICAL FLANGE PLUG, HELICAL FLANGE SEAT AND HELICAL FLANGE REDUCTION SEAT
INTERPORE CROSS INTL.
K031772
06/09/2003
TI FENESTRATED PLATE
INTERPORE CROSS INTL.
K041794
07/02/2004
C-TEK C-THRU ANTERIOR CERVICAL PLATE SYSTEM
INTERPORE CROSS INTL.
K042798
10/08/2004
C-TEK C-TRUN ANTERIOR CERVICAL PLATE SYSTEM
INTERPORE CROSS INTL.
K043229
11/22/2004
MODIFICATION TO ALTIUS OCT SYSTEM
INTERPORE CROSS INTL.
K033961
12/22/2003
ALTIUS OCT SYSTEM
INTERPORE CROSS INTL.
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