510(k) · Cleared

Cleared

Captiva Spine SmartLOX Cervical Plate System

K141332510(k) TraditionalCleared Jun 11, 2015386-day reviewClass II21 CFR 888.3060

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

Captiva Spine · KWQ Appliance, Fixation, Spinal Intervertebral Body

Cleared on Jun 11, 2015 as substantially equivalent to K032815 (Precision Surgery Limited, 2004) and 2 other predicates after a 386-day review. Its family tree reaches back 2 generations to 1979. 1 later device descends from it.

Decided: Jun 11, 2015
Review: 386 days
Class: Class II
Product code: KWQ
Recalls: None
Predicates: 3

Its longest line of descent runs back 2 generations to K792352 (1979). 6 ancestors in all. 1 later device descends from it, 1 citing it directly.

By dateBy generation

Root · 2 generations backK792352 Synthes Cervical Vertabrae PlatesDePuy Synthes · 1979
1 generation backK042499 Orion Anterior Cervical Plating SystemMedtronic Sofamor Danek · 2004
This deviceK141332 Captiva Spine SmartLOX Cervical Plate SystemCaptiva Spine · 2015
Descendant · cites it directly · 0 of its ownK200301 UNiTi ACDF Implant SystemPressio, Inc. · 2021

Most influential descendants

Showing 1 of 1 · See all

K200301UNiTi ACDF Implant SystemPressio, Inc. · 2021 · cites it directly0descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−2	K792352	Synthes Cervical Vertabrae Plates	DePuy Synthes	1979	—
−1	K042499	Orion Anterior Cervical Plating System	Medtronic Sofamor Danek	2004	—
0 (this device)	K141332	Captiva Spine SmartLOX Cervical Plate System	Captiva Spine	2015	—
+1	K200301	UNiTi ACDF Implant System	Pressio, Inc.	2021	—

Other ancestors by year cleared

Year cleared	Devices	With a Class I recall
1980	1	0
1998	1	0
2004	1	0
2008	1	0

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2021	1	0

FIG. 1 — Lineage of K141332, 1979–2021Source: 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 KWQ? 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 KWQ device

#1 K233640 Segmental Plating System (SPS);IdentiTi SPS…score 21.9 · 31 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
*	K032815	Precision Surgery Limited Variable and Fixed Cervical Plate System Summary page 5 …LOX Cervical Plate System is substantially equivalent to the previously cleared Precision Surgery Ltd. Fixed, Variable and Corpectomy Cervical Plate System found in both K032815 and K073708 (primary predicate) and Medtronic Sofamor Danek Orion Anterior Cervical Plate System cleared per K042499. Performanc…	Precision Surgery Limited	2004	—
*	K073708	Fixed, Variable & Corpectomy Cervical Plate System Summary page 5 …Plate System is substantially equivalent to the previously cleared Precision Surgery Ltd. Fixed, Variable and Corpectomy Cervical Plate System found in both K032815 and K073708 (primary predicate) and Medtronic Sofamor Danek Orion Anterior Cervical Plate System cleared per K042499. Performance Standards:…	Precision Surgery, Ltd.	2008	3
*	K042499	Orion Anterior Cervical Plating System Summary page 5 …e and Corpectomy Cervical Plate System found in both K032815 and K073708 (primary predicate) and Medtronic Sofamor Danek Orion Anterior Cervical Plate System cleared per K042499. Performance Standards: Captiva Spine SmartLOX Cervical Plate System was evaluated to demonstrate equivalence to the predicate d…	Medtronic Sofamor Danek	2004	—

Also cleared against K032815: 2 other devices →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

Number	Device	Applicant	Decided	Descendants
K200301	UNiTi ACDF Implant System	Pressio, Inc.	2021	0

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?

The line of descent spans 36 years and passes through 3 companies; a new generation was cleared every 24.8 years on median.
1 of the 6 ancestors has a recall of any class.
Of its descendants, K200301 (Pressio, Inc., 2021) has gone furthest, with 0 descendants of its own.
2 other devices also cite its predicate K032815.

How does its category compare?

All KWQ devices

KWQ Appliance, Fixation, Spinal Intervertebral Body: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.

FDA decisions per year · KWQ

7in 2025

2007high 32 (2008) · low 7 (2025)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KWQ

64in 2025

2007high 124 (2014) · low 55 (2020)2026

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

Recalls per year · KWQ

1in 2018

2007high 35 (2009) · low 0 (2014)2026

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

Adverse event reports per year · KWQ

248in 2025

2007high 796 (2013) · low 248 (2025)2025

MAUDE reports naming product code KWQ, 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	27	101	2	288
2008	32	70	33	348
2009	23	90	35	355
2010	23	104	2	691
2011	22	95	5	415
2012	26	90	7	544
2013	22	88	6	796
2014	17	124	0	546
2015	25	102	2	562
2016	15	121	9	502
2017	20	67	8	492
2018	22	95	1	341
2019	26	81	0	298
2020	26	55	0	400
2021	17	59	0	591
2022	18	85	0	392
2023	16	59	0	320
2024	17	64	0	419
2025	7	64	0	248
2026	10	76	0	—

What is it indicated for?

The Captiva Spine SmartLOX Cervical Plate System is intended for anterior screw fixation of the cervical spine. These implants have been designed to provide stabilization as an adjunct to cervical fusion. Indications for the use of this implant system include degenerative disc disease defined as neck pain of discogenic origin with the degeneration of the disc confirmed by history and radiographic studies, spondylolisthesis, trauma, spinal stenosis, deformity, tumor, pseudoarthrosis or failed previous fusion. WARNING: The Captiva Spine SmartLOX Cervical Plate System is not intended for screw attachment or fixation to the posterior elements (pedicles) of the cervical, thoracic or lumbar spine.

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K141332 · printed Nov 6, 2026

Cite this page

510(k) Report. “K141332: Captiva Spine SmartLOX Cervical Plate System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K141332

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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