The following data is part of a premarket notification filed by Osteotech, Inc. with the FDA for Grafton Dbm.
Device ID | K051195 |
510k Number | K051195 |
Device Name: | GRAFTON DBM |
Classification | Filler, Bone Void, Osteoinduction (w/o Human Growth Factor) |
Applicant | OSTEOTECH, INC. 51 JAMES WAY Eatontown, NJ 07724 |
Contact | Christopher W Talbot |
Correspondent | Christopher W Talbot OSTEOTECH, INC. 51 JAMES WAY Eatontown, NJ 07724 |
Product Code | MBP |
CFR Regulation Number | 888.3045 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-05-10 |
Decision Date | 2005-12-16 |
Summary: | summary |