DBX DEMINERALIZED BONE MATRIX PUTTY, BONE MATRIX PASTE AND BONE MATRIX MIX— 510(k) K040262
Substantially EquivalentMusculoskeletal Transplant Foundation
FDA 510(k) clearance K040262 for DBX DEMINERALIZED BONE MATRIX PUTTY, BONE MATRIX PASTE AND BONE MATRIX MIX, Substantially Equivalent on 2005-03-17. Applicant: Musculoskeletal Transplant Foundation. Device class: 2.
Clearance details
- Applicant
- Musculoskeletal Transplant Foundation
- Product code
- Code MQV
- Device class
- Class 2
- Regulation
- 21 CFR 888.3045
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Edison, NJ, US
Recent devices under product code MQV
view allMore clearances from Musculoskeletal Transplant Foundation
view allAdverse events under product code MQV
product code MQV- Death
- 6
- Injury
- 435
- Total
- 441
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recalls naming K040262
K-number listed on FDA's recall record- Z-0323-2024 — DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous defects created from traumatic injury. Model Number: 038100
- Z-1455-2015 — DBX Mix, 20 cc, Product Code: 058200. Demineralized Bone Matrix Mix, bone void filler.
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K040262.
Data sourced from openFDA. This site is unofficial and independent of the FDA.