FDA 510(k) Applications Submitted by JANICE L FILIPPELLI

FDA 510(k) Number Submission Date Device Name Applicant
K930592 02/04/1993 ACE UNIVERSAL RECONSTRUCTION PLATE ACE MEDICAL CO.
K931652 04/05/1993 ACE 6.5 MM BONE SCREW ACE MEDICAL CO.
K920738 02/19/1992 ACE 100 DEGREES TUBULAR PLATE ACE ORTHOPEDIC MANUFACTURING CO.
K980696 02/23/1998 FOAM TIP INJECTOR STAAR SURGICAL CO.
K926047 12/01/1992 ACE 8.0MM CANNULATED CANCELLOUS BONE SCREW ACE ORTHOPEDIC MANUFACTURING CO.


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