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FDA 510(k) Applications Submitted by CERAMED CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K960348
01/25/1996
OSTEOGRAF/N-300 HYDROXYLAPATITE
CERAMED CORP.
K960349
01/25/1996
PERMARIDGE HYDROXYLAPATITE MATRIX
CERAMED CORP.
K960353
01/25/1996
OSTEOGRAF/LD-300 HYDROXYLAPATITE
CERAMED CORP.
K960354
01/25/1996
PERMAMESH-D HYDROXYLAPATITE MATRIX
CERAMED CORP.
K960361
01/25/1996
PERMAMESH-D HYDROXYLAPATITE MATRIX
CERAMED CORP.
K960362
01/25/1996
PERMAMESH HYDROXYLAPATITE MATRIX
CERAMED CORP.
K960368
01/25/1996
OSTEOGRAFT/N-700 HYDROXYLAPTITE
CERAMED CORP.
K962786
07/17/1996
OSTEOGRAF STAINLESS STEEL SYRING
CERAMED CORP.
K962838
07/22/1996
PERMARIDGE SYRINGE
CERAMED CORP.
K954631
10/06/1995
OSTEOGRAF/N-BLOCCK HYDROXYLAPATITE
CERAMED CORP.
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