510(k) Report

510(k) · Cleared

Cleared

DBX Demineralized Bone Matrix Mix

K063676510(k) TraditionalCleared Mar 5, 200784-day reviewClass II21 CFR 888.3045

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Musculoskeletal Transplant Foundation · MBP Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)

Cleared on Mar 5, 2007 after an 84-day review. The FDA summary names no predicate by number. 5 later devices descend from it.

Decided
Mar 5, 2007
Review
84 days
Class
Class II
Product code
MBP
Recalls
None
Predicates
0

5 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2012: 1 descendant cleared2009: 1 descendant cleared2021: 1 descendant cleared2025: 1 descendant cleared2023: 1 descendant cleared20052010201520202025
  1. This deviceK063676 DBX Demineralized Bone Matrix MixMusculoskeletal Transplant Foundation · 2007
  2. Descendant · cites it directly · 2 of its ownK091193 Accell EVO3CIsotis Orthobiologics, Inc. · 2009 · Recalled
  3. Descendant · 2 generations on · 1 of its ownK212135 Dry DBM- A PuttySeaspine Corporation · 2021
  4. Descendant · cites it directly · 1 of its ownK121989 Optecure Bone Void Filler (0.5 CC, 1CC, 2CC, 5CC, 10CC, and 20CC)…Exactech, Inc. · 2012
  5. Descendant · 2 generations on · 0 of its ownK241555 Moldable Bone Void Filler and Moldable Bone Void Filler + CCCRti Surgical, Inc. · 2025
  6. Descendant · 3 generations on · 0 of its ownK231030 Cove Putty, OsteoCove PuttySeaSpine Orthopedics Corporation · 2023

Most influential descendants

Showing 5 of 5 · See all
  • K091193Accell EVO3CIsotis Orthobiologics, Inc. · 2009 · cites it directly2descendants
  • K212135Dry DBM- A PuttySeaspine Corporation · 2021 · 2 generations on1descendant
  • K121989Optecure Bone Void Filler (0.5 CC, 1CC, 2CC, 5CC, 10CC, and 20CC), Optecure + CCC Bone…Exactech, Inc. · 2012 · cites it directly1descendant
  • K241555Moldable Bone Void Filler and Moldable Bone Void Filler + CCCRti Surgical, Inc. · 2025 · 2 generations on0descendants
  • K231030Cove Putty, OsteoCove PuttySeaSpine Orthopedics Corporation · 2023 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K063676DBX Demineralized Bone Matrix MixMusculoskeletal Transplant Foundation2007—
+1K091193Accell EVO3CIsotis Orthobiologics, Inc.20091
+2K212135Dry DBM- A PuttySeaspine Corporation2021—
+1K121989Optecure Bone Void Filler (0.5 CC, 1CC, 2CC, 5CC, 10CC, and 20CC), Optecure +…Exactech, Inc.2012—
+2K241555Moldable Bone Void Filler and Moldable Bone Void Filler + CCCRti Surgical, Inc.2025—
+3K231030Cove Putty, OsteoCove PuttySeaSpine Orthopedics Corporation2023—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200910
201210
202110
202310
202510
FIG. 1 — Lineage of K063676, 2007–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in MBP? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new MBP device

  1. #1 K242799 PliaFX Floscore 9.0 · 3 generations · no Class I recall
Get a 510(k) Report

What was it cleared against?

The FDA summary names no predicate by number.

What descends from it? (5)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K091193Accell EVO3CIsotis Orthobiologics, Inc.20092
K121989Optecure Bone Void Filler (0.5 CC, 1CC, 2CC, 5CC, 10CC, and 20CC), Optecure + CCC Bone…Exactech, Inc.20121

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K091193 (Isotis Orthobiologics, Inc., 2009) has gone furthest, with 2 descendants of its own.

How does its category compare?

All MBP devices

MBP Filler, Bone Void, Osteoinduction (W/O Human Growth Factor): FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.

FDA decisions per year · MBP

1in 2024

2007: 52008: 52009: 12011: 12012: 12013: 32015: 12024: 1
2007high 5 (2007) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MBP

181in 2013

2007: 188 days median2008: 93 days median2013: 181 days median
2007high 188 (2007) · low 93 (2008)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · MBP

7in 2023

2011: 22012: 132014: 12016: 12023: 72026 (partial year): 2
2007high 13 (2012) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · MBP

2in 2025

2007: 72008: 152009: 92010: 142011: 182012: 242013: 162014: 152015: 112016: 62017: 52018: 92019: 32020: 62021: 22022: 42023: 62024: 12025: 2
2007high 24 (2012) · low 1 (2024)2025

MAUDE reports naming product code MBP, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007518807
2008593015
20091—09
20100—014
20111—218
20121—1324
20133181016
20140—115
20151—011
20160—16
20170—05
20180—09
20190—03
20200—06
20210—02
20220—04
20230—76
20241—01
20250—02
20260—2—

What is it indicated for?

DBX® is intended for use as a Demineralized Bone Matrix for voids or gaps that are not intrinsic to the stability of the bony structure. It can be used in the:

Putty: Extremities, Pelvis, Posterolateral Spine, Cranium

Mix: Extremities, Pelvis, Spine

Paste: Extremities

DBX® is indicated for treatment of surgically created osseous defects or osseous defects created from traumatic injury.

DBX®Putty can be used as an extender in the spine with autograft. DBX®Mix may be used as a bone void filler in the spine. DBX® can be used with bone marrow.

DBX® is for single patient use only.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K063676: DBX Demineralized Bone Matrix Mix.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K063676

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026