FDA 510(k) Applications Submitted by OSTEOGENICS BIOMEDICAL, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K003028 |
09/28/2000 |
CYTOPLAST SUTURE; CS-0318, CS-0416, CS-0418, CS-0513, CS-0513PC, CS-0516HC |
OSTEOGENICS BIOMEDICAL, INC. |
| K072076 |
07/30/2007 |
CYTOPLAST PTFE SUTURE |
OSTEOGENICS BIOMEDICAL, INC. |
| K093719 |
12/02/2009 |
PRO-FIX PRECISION FIXATION SYSTEM MODEL PFM#, PFB#, PFT# |
OSTEOGENICS BIOMEDICAL, INC. |
| K993610 |
10/25/1999 |
CYTOPLAST RESORB, MODELS R-250, RP-250, RU-250, RPS-250, RPL-250 |
OSTEOGENICS BIOMEDICAL, INC. |
| K013764 |
11/13/2001 |
IMMIX BONE GRAFT EXTENDER |
OSTEOGENICS BIOMEDICAL, INC. |
| K984230 |
11/25/1998 |
OSTEO-MESH TM-300 |
OSTEOGENICS BIOMEDICAL, INC. |
| K201187 |
05/01/2020 |
Cytoplast Titanium-Reinforced PTFE Membranes |
Osteogenics Biomedical, Inc. |
| K171774 |
06/14/2017 |
RPM Reinforced PTFE Mesh |
Osteogenics Biomedical, Inc. |
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