DBX Demineralized Bone Matrix Putty
FDA 510(k) K103784 · Musculoskeletal Transplant Foundation
510(k) numberK103784
Submission
- Device name
- DBX Demineralized Bone Matrix Putty
- Applicant
- Musculoskeletal Transplant Foundation
Edison, NJ, US - Received
- December 27, 2010
- Decision date
- April 13, 2011
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MQV – Filler, Bone Void, Calcium Compound
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3045
- Specialty
- Orthopedic
- Implant
- Yes
Other 510(k)s with product code MQV
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K262230 | Mg OSTEOREVIVE;Mg OSTEOCRETEMQV · Traditional | Bone Solutions, Inc. | 09/11/2026SE |
| K260364 | Device 300419 StripMQV · Traditional | Geistlich Pharma AG | 06/02/2026SE |
| K252797 | JAZBI Resorbable Bone Void FillerMQV · Traditional | Sdip Innovations Pty, Ltd. | 05/26/2026SE |
| K261008 | Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip; Vitoss® BiModal Bioactive…MQV · Special | Stryker Spine | 04/24/2026SE |
| K253524 | Adaptos®Fuse Bone GraftMQV · Traditional | Biomendex OY | 02/17/2026SE |
| K253147 | FIBERGRAFT BG Putty GPS Bone Graft Substitute FIBERGRAFT BG Putty Bone Graft…MQV · Special | Prosidyan, Inc. | 10/22/2025SE |
| K251522 | Mg OSTEOINJECT; Mg OSTEOREVIVE; Mg OSTEOCRETEMQV · Traditional | Bone Solutions, Inc. | 10/13/2025SE |
| K252085 | Allomatrix (Allomatrix Injectable Putty; Allomatrix C; Allomatrix DR; Allomatrix Custom)MQV · Traditional | Wright Medical Technology, Inc. (Stryker… | 09/30/2025SE |
| K251556 | Device 300423 GranulesMQV · Traditional | Geistlich Pharma AG | 07/17/2025SE |
| K251720 | OsteoFlo HydroFiberMQV · Special | SurGenTec, LLC | 07/02/2025SE |
More from SurGenTec, LLC
| 510(k) | Device | Decision |
|---|---|---|
| K181633 | MTF Pre-Sutured TendonGAT · Traditional | 03/15/2019SE |
| K121313 | MTF New Bone Void FillerMQV · Traditional | 01/11/2013SE |
| K120479 | MTF FasciaOWY · Traditional | 11/08/2012SE |
| K113167 | MTF New Bone Voild FillerMQV · Traditional | 01/24/2012SE |
| K110003 | MTF New Bone Void FillerMQV · Traditional | 10/13/2011SE |
| K103795 | DBX Demineralized Bone Matrix PuttyMQV · Traditional | 04/13/2011SE |
| K091217 | DBX Demineralized Bone Matrix PuttyNUN · Traditional | 10/02/2009SE |
| K091218 | DBX Demineralized Bone Matrix PuttyMQV · Traditional | 09/28/2009SE |
| K080399 | DBX Demineralized Bone Matrix Putty, DBX Demineralized Bone Matrix PasteMBP · Traditional | 10/10/2008SE |
| K080405 | Sygnal DBMMBP · Traditional | 08/28/2008SE |
Questions and answers
When was DBX Demineralized Bone Matrix Putty cleared by the FDA?
DBX Demineralized Bone Matrix Putty (K103784) received a 510(k) decision of Substantially Equivalent on April 13, 2011, 107 days after the submission was received.
What is the product code of K103784?
The FDA product code is MQV – Filler, Bone Void, Calcium Compound, a Class II (moderate risk) device regulated under 21 CFR 888.3045.