510(k) · Cleared

Cleared

Osteofix Bone Void Filler

K070220510(k) TraditionalCleared Apr 12, 200779-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

Calcitec, Inc. · MQV Filler, Bone Void, Calcium Compound

Cleared on Apr 12, 2007 as substantially equivalent to K990131 (Interpore Cross Intl., 1999) and 2 other predicates after a 79-day review. Its family tree reaches back 1 generation to 1999.

Decided: Apr 12, 2007
Review: 79 days
Class: Class II
Product code: MQV
Recalls: None
Predicates: 3

Its longest line of descent runs back 1 generation to K990131 (1999). 3 ancestors in all. No later device cites it as a predicate yet.

By dateBy generation

Root · 1 generation backK990131 Pro Osteon Implant 500R Resorbable Bone Graft SubstituteInterpore Cross Intl. · 1999
This deviceK070220 Osteofix Bone Void FillerCalcitec, Inc. · 2007

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−1	K990131	Pro Osteon Implant 500R Resorbable Bone Graft Substitute	Interpore Cross Intl.	1999	—
0 (this device)	K070220	Osteofix Bone Void Filler	Calcitec, Inc.	2007	—

Other ancestors by year cleared

Year cleared	Devices	With a Class I recall
2001	1	0
2004	1	0

FIG. 1 — Lineage of K070220, 1999–2007Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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 MQV? 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 MQV device

#1 K232315 Catalyst Bone Void Fillerscore 25.2 · 25 generations · no Class I recall
#2 Held for the reportin the report
#3 Held for the reportin the report

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What was it cleared against? (3)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

Type	Number	Device	Applicant	Decided	Recalls
*	K990131	Pro Osteon Implant 500R Resorbable Bone Graft Substitute Summary page 1 …Classification: Class II Classification Name: Filler, bone void, calcium compound Predicate Devices * Interpore CrosslInternational, Pro Osteon5SOOR (K990131) * Berkeley Advanced Biomaterials, Inc., Cem-Ostetic (K040405) * Synthes, Norian SRS Bone Void Filler (KOl11897) Inten…	Interpore Cross Intl.	1999	—
*	K040405	Cem-Ostetic Putty Injection Kit, Model Pik-XX, Pik-XX-YY Summary page 1 …bone void, calcium compound Predicate Devices * Interpore CrosslInternational, Pro Osteon5SOOR (K990131) * Berkeley Advanced Biomaterials, Inc., Cem-Ostetic (K040405) * Synthes, Norian SRS Bone Void Filler (KOl11897) Intended Use / Indications for Use OsteofiXTm Bone Void Filler is indic…	Berkeley Advanced Biomaterials, Inc.	2004	—
*	K011897	Norian SRS Bone Void Filler	Synthes (Usa)	2001	—

Also cleared against K990131: 17 other devices →

What descends from it?

No later submission names this one as a predicate yet.

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?

None of the 3 ancestors has a recall.
17 other devices also cite its predicate K990131.

How does its category compare?

All MQV devices

MQV Filler, Bone Void, Calcium Compound: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.

FDA decisions per year · MQV

14in 2025

2007high 35 (2007) · low 8 (2016)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MQV

57in 2025

2007high 214 (2016) · low 55 (2024)2026

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

Recalls per year · MQV

1in 2025

2007high 6 (2011) · low 0 (2010)2026

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

Adverse event reports per year · MQV

57in 2025

2007high 223 (2013) · low 47 (2022)2025

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

View these four charts as a table

Year	Decisions	Median 510(k) review, days	Recalls (Class I)	MAUDE reports
2007	35	144	5	67
2008	32	102	3	71
2009	23	180	1	81
2010	17	147	0	68
2011	16	92	6	114
2012	9	107	3	149
2013	12	197	2	223
2014	20	153	0	111
2015	18	184	0	125
2016	8	214	1	106
2017	17	124	1	107
2018	23	124	2	86
2019	13	90	0	65
2020	15	132	1	126
2021	8	88	0	101
2022	9	118	0	47
2023	21	74	3	120
2024	28	55	2	68
2025	14	57	1	57
2026	5	96	4	—

What is it indicated for?

OsteofixTM Bone Void Filler is indicated for use to fill bony voids or gaps that are not intrinsic to the stability of the bony structure. OsteofixTM Bone Void Filler is intended to be injected into bony voids or gaps of the skeletal system (i.e., the extremities, spine and pelvis). These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. The product provides a Bone Void Filler that resorbs and is replaced with bone during the healing process.

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K070220 · printed Nov 6, 2026

Cite this page

510(k) Report. “K070220: Osteofix Bone Void Filler.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K070220

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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