Osteotech, Inc.
FDA 510(k) medical device clearances.
Top product codes for Osteotech, Inc.
Recent clearances by Osteotech, Inc.
- K082615 — GRAFTON R II EDBM, DEMINERALIZED BONE MATRIX ALLOGRAFT, RESORBABLE CALCIUM SALT BONE VOID FILLER DEVICES
- K081227 — PLEXUR M
- K080511 — PLEXUR-P
- K073405 — PLEXUR M
- K061982 — PLEXUR P
- K051188 — GRAFTON DBM
- K051195 — GRAFTON DBM
- K051781 — GRAFTCAGE TLX
- K043209 — VIAGRAF DBM PASTE
- K053080 — GRAFTCAGE ACX
- K042707 — GRAFTON PLUS DBM PASTE
- K043048 — GRAFTON PLUS DBM PASTE
- K012254 — VBR
- K003155 — VERTEBRAL BODY REPLACEMENT
- K003384 — VERSALINK TITANIUM ROD-TO-ROD COUPLERS
- K992885 — VERSALOK LOW BACK FIXATION SYSTEM
- K991586 — SSCS (SEGMENTAL SPINAL CORRECTION SYSTEM)
- K973868 — SSCS (SEGMENTAL SPINAL CORRECTION SYSTEM)
- K971289 — SSCS (SEGMENTAL SPINAL CORRECTION SYSTEM)
- K955173 — SSCS (SEGMENTAL SPINAL CORRECTION SYSTEM)
- K950652 — OSTEOTECH NAVICULAR AND CANCELLOUS CANNULATED SCREWS
- K951811 — OSTEOTECH MUSCULOSKELETAL TISSUE RECOVERY PACK
- K883065 — ALLOPREP SYSTEM
- K852199 — OSTEOGRAF 2040 OSTEOGRAF 4060
Data sourced from openFDA. This site is unofficial and independent of the FDA.