Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Osteotech, Inc.

FDA 510(k) & PMA Approved Devices — 24 products

Total Devices24
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K082615 GRAFTON R II EDBM, DEMINERALIZED BONE MATRIX ALLOGRAFT, RESORBABLE CALCIUM SALT BONE VOID FILLER DEVICESMQV2008-10-16 View
510(k) K081227 PLEXUR MMQV2008-07-22 View
510(k) K080511 PLEXUR-PMQV2008-04-21 View
510(k) K073405 PLEXUR MMQV2008-03-03 View
510(k) K061982 PLEXUR PMBP2007-02-07 View
510(k) K051188 GRAFTON DBMNUN2006-01-03 View
510(k) K051195 GRAFTON DBMMBP2005-12-16 View
510(k) K051781 GRAFTCAGE TLXMQP2005-12-16 View
510(k) K043209 VIAGRAF DBM PASTEMBP2005-12-05 View
510(k) K053080 GRAFTCAGE ACXMQP2005-12-01 View
510(k) K042707 GRAFTON PLUS DBM PASTENUN2005-11-30 View
510(k) K043048 GRAFTON PLUS DBM PASTEMBP2005-11-23 View
510(k) K012254 VBRMQP2001-10-16 View
510(k) K003155 VERTEBRAL BODY REPLACEMENTMQP2001-01-04 View
510(k) K003384 VERSALINK TITANIUM ROD-TO-ROD COUPLERSMNH2000-11-24 View
510(k) K992885 VERSALOK LOW BACK FIXATION SYSTEMKWP1999-11-19 View
510(k) K991586 SSCS (SEGMENTAL SPINAL CORRECTION SYSTEM)KWP1999-07-23 View
510(k) K973868 SSCS (SEGMENTAL SPINAL CORRECTION SYSTEM)KWP1998-01-08 View
510(k) K971289 SSCS (SEGMENTAL SPINAL CORRECTION SYSTEM)KWP1997-06-18 View
510(k) K955173 SSCS (SEGMENTAL SPINAL CORRECTION SYSTEM)KWP1996-02-09 View
↑