510(k) Report

510(k) · Cleared

Cleared

Anterior Cervical Plate System

K151553510(k) TraditionalCleared Feb 10, 2016246-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

Osteomed Implantes, Ltda · KWQ Appliance, Fixation, Spinal Intervertebral Body

Cleared on Feb 10, 2016 as substantially equivalent to K031276 (Synthes (Usa), 2003) and 8 other predicates after a 246-day review. Its family tree reaches back 5 generations to 1995. 11 later devices descend from it.

Decided
Feb 10, 2016
Review
246 days
Class
Class II
Product code
KWQ
Recalls
None
Predicates
9

Its longest line of descent runs back 5 generations to K953730 (1995). 18 ancestors in all, the oldest K914362 (1992). 11 later devices descend from it, 4 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2010: 1 other ancestor2008: 1 other ancestor2004: 2 other ancestors2003: 2 other ancestors2000: 2 other ancestors1995: 1 other ancestor2007: 1 other ancestor2006: 1 other ancestor1992: 1 other ancestor1997: 1 other ancestor2017: 2 descendants cleared2021: 2 descendants cleared2016: 1 descendant cleared2020: 1 descendant cleared2025: 1 descendant cleared2026: 4 descendants clearedK953730 · Codman Anterior Cervical Plate System · Johnson & Johnson Professionals, Inc. · 1995K013877 · Codman Slim-Loc System · Codman & Shurtleff, Inc. · 2001K040655 · Swift Anterior Cervical Plate System · Depuy Spine, Inc. · 2004K072546 · Swift Plus Anterior Cervical Plate System · Depuy Spine, Inc. · 2007K080646 · C-Tek Maxan Anterior Cervical Plate System · Biomet Spine · 2008 · recalled1990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 8 other ancestors2 generations back: 4 other ancestors3 generations back: 1 other ancestor 1 generation forward: 4 descendants2 generations forward: 3 descendants3 generations forward: 3 descendants4 generations forward: 1 descendant K080646 · C-Tek Maxan Anterior Cervical Plate System · Biomet Spine · 2008 · recalledK072546 · Swift Plus Anterior Cervical Plate System · Depuy Spine, Inc. · 2007K040655 · Swift Anterior Cervical Plate System · Depuy Spine, Inc. · 2004K013877 · Codman Slim-Loc System · Codman & Shurtleff, Inc. · 2001K953730 · Codman Anterior Cervical Plate System · Johnson & Johnson Professionals, Inc. · 1995−50
  1. Root · 5 generations backK953730 Codman Anterior Cervical Plate SystemJohnson & Johnson Professionals, Inc. · 1995
  2. 4 generations backK013877 Codman Slim-Loc SystemCodman & Shurtleff, Inc. · 2001
  3. 3 generations backK040655 Swift Anterior Cervical Plate SystemDepuy Spine, Inc. · 2004
  4. 2 generations backK072546 Swift Plus Anterior Cervical Plate SystemDepuy Spine, Inc. · 2007
  5. 1 generation backK080646 C-Tek Maxan Anterior Cervical Plate SystemBiomet Spine · 2008 · Recalled
  6. This deviceK151553 Anterior Cervical Plate SystemOsteomed Implantes, Ltda · 2016
  7. Descendant · cites it directly · 8 of its ownK161524 Tangis Anterior Cervical PlateNvision Biomedical Technologies, LLC · 2016
  8. Descendant · cites it directly · 4 of its ownK210424 Quantum Anterior Cervical PlateNvision Biomedical Technologies, Inc. · 2021
  9. Descendant · 2 generations on · 3 of its ownK252611 aprevo® cervical plating systemCarlsmed, Inc. · 2025
  10. Descendant · 3 generations on · 1 of its ownK260570 corra™ cervical plating systemCarlsmed, Inc. · 2026
  11. Descendant · 2 generations on · 1 of its ownK202657 Javelin Tailor's Bunion Fixation SystemNvision Biomedical Technologies, Inc. · 2020

Showing 5 of 11 descendants. See all descendants

Descendants cleared per year

2016: 12017: 22020: 12021: 22025: 12026: 4
2016high 4 (2026) · low 0 (2018)2026

Most influential descendants

Showing 5 of 11 · See all
  • K161524Tangis Anterior Cervical PlateNvision Biomedical Technologies, LLC · 2016 · cites it directly8descendants
  • K210424Quantum Anterior Cervical PlateNvision Biomedical Technologies, Inc. · 2021 · cites it directly4descendants
  • K252611aprevo® cervical plating systemCarlsmed, Inc. · 2025 · 2 generations on3descendants
  • K260570corra™ cervical plating systemCarlsmed, Inc. · 2026 · 3 generations on1descendant
  • K202657Javelin Tailor's Bunion Fixation SystemNvision Biomedical Technologies, Inc. · 2020 · 2 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K953730Codman Anterior Cervical Plate SystemJohnson & Johnson Professionals, Inc.1995—
−4K013877Codman Slim-Loc SystemCodman & Shurtleff, Inc.2001—
−3K040655Swift Anterior Cervical Plate SystemDepuy Spine, Inc.2004—
−2K072546Swift Plus Anterior Cervical Plate SystemDepuy Spine, Inc.2007—
−1K080646C-Tek Maxan Anterior Cervical Plate SystemBiomet Spine20082
0 (this device)K151553Anterior Cervical Plate SystemOsteomed Implantes, Ltda2016—
+1K161524Tangis Anterior Cervical PlateNvision Biomedical Technologies, LLC2016—
+1K210424Quantum Anterior Cervical PlateNvision Biomedical Technologies, Inc.2021—
+2K252611aprevo® cervical plating systemCarlsmed, Inc.2025—
+3K260570corra™ cervical plating systemCarlsmed, Inc.2026—
+2K202657Javelin Tailor's Bunion Fixation SystemNvision Biomedical Technologies, Inc.2020—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199210
199510
199710
200020
200320
200420
200610
200710
200810
201010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
201720
202010
202120
202510
202640
FIG. 1 — Lineage of K151553, 1995–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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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 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. #1 K233640 Segmental Plating System (SPS);IdentiTi SPS…score 21.9 · 31 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (9)

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.

TypeNumberDeviceApplicantDecidedRecalls
*K031276Synthes Anterior Cervical Locking Plate (Aclp) System
Summary page 4
…KWQ CFR Section 21 CFR section 888.3060 Device Panel Orthopedic Primary Predicate Cervical Spine Locking Plate (CSLP) - Synthes (K031276/K030866/K000742/ Device K000536/K945700) C-Tek MaxAn Anterior Cervical Plate System…
Synthes (Usa)2003—
*K030866Synthes Anterior CSLP System
Summary page 4
…CFR Section 21 CFR section 888.3060 Device Panel Orthopedic Primary Predicate Cervical Spine Locking Plate (CSLP) - Synthes (K031276/K030866/K000742/ Device K000536/K945700) C-Tek MaxAn Anterior Cervical Plate System - Biome…
Synthes (Usa)2003—
*K000742Synthes Anterior CSLP System
Summary page 4
…ion 21 CFR section 888.3060 Device Panel Orthopedic Primary Predicate Cervical Spine Locking Plate (CSLP) - Synthes (K031276/K030866/K000742/ Device K000536/K945700) C-Tek MaxAn Anterior Cervical Plate System - Biomet Spine…
Synthes Spine2000—
*K000536Synthes Anterior CSLP System
Summary page 4
…8.3060 Device Panel Orthopedic Primary Predicate Cervical Spine Locking Plate (CSLP) - Synthes (K031276/K030866/K000742/ Device K000536/K945700) C-Tek MaxAn Anterior Cervical Plate System - Biomet Spine (K080646) Additional Predicate…
Synthes Spine20001
*K945700Synthes (Usa) Anterior Cervical Vertebrae Plate System
Summary page 4
…Device Panel Orthopedic Primary Predicate Cervical Spine Locking Plate (CSLP) - Synthes (K031276/K030866/K000742/ Device K000536/K945700) C-Tek MaxAn Anterior Cervical Plate System - Biomet Spine (K080646) Additional Predicate…
Synthes (Usa)1995—
*K080646C-Tek Maxan Anterior Cervical Plate System
Summary page 4
…SLP) - Synthes (K031276/K030866/K000742/ Device K000536/K945700) C-Tek MaxAn Anterior Cervical Plate System - Biomet Spine (K080646) Additional Predicate UNIPLATE ANTERIOR CERVICAL PLATE, - DePuy (K042544 / K082273 / Devices…
Biomet Spine20082
*K042544Uniplate Anterior Cervical Plate System
Summary page 4
…C-Tek MaxAn Anterior Cervical Plate System - Biomet Spine (K080646) Additional Predicate UNIPLATE ANTERIOR CERVICAL PLATE, - DePuy (K042544 / K082273 / Devices K100070) The Osteomed Implantes Anterior Cervical Plate…
Depuy Spine, Inc.2004—
*K082273Uniplate Anterior Cervical Plate System
Summary page 4
…C-Tek MaxAn Anterior Cervical Plate System - Biomet Spine (K080646) Additional Predicate UNIPLATE ANTERIOR CERVICAL PLATE, - DePuy (K042544 / K082273 / Devices K100070) The Osteomed Implantes Anterior Cervical Plate System is…
Depuy Spine, Inc.2008—
*K100070Uniplate Anterior Cervical Plate System
Summary page 4
…- Biomet Spine (K080646) Additional Predicate UNIPLATE ANTERIOR CERVICAL PLATE, - DePuy (K042544 / K082273 / Devices K100070) The Osteomed Implantes Anterior Cervical Plate System is intended for anterior…
Depuy Spine, Inc.2010—

Also cleared against K031276: 13 other devices →

What descends from it? (11)

See all 11

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

NumberDeviceApplicantDecidedDescendants
K161524Tangis Anterior Cervical PlateNvision Biomedical Technologies, LLC20168
K210424Quantum Anterior Cervical PlateNvision Biomedical Technologies, Inc.20214
K210325APOLLO Anterior Cervical Plate (ACP) SystemAurora Spine, Inc.20210
K172585Liberty Anterior Cervical PlateValorus Spine20170

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 21 years and passes through 5 companies; a new generation was cleared every 3.3 years on median.
  • 2 of the 18 ancestors have a recall of any class.
  • Of its descendants, K161524 (Nvision Biomedical Technologies, LLC, 2016) has gone furthest, with 8 descendants of its own.
  • 13 other devices also cite its predicate K031276.

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. 2016, this device’s year, is highlighted.

FDA decisions per year · KWQ

7in 2025

2007: 272008: 322009: 232010: 232011: 222012: 262013: 222014: 172015: 252016: 152017: 202018: 222019: 262020: 262021: 172022: 182023: 162024: 172025: 72026 (partial year): 10
2007high 32 (2008) · low 7 (2025)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KWQ

64in 2025

2007: 101 days median2008: 70 days median2009: 90 days median2010: 104 days median2011: 95 days median2012: 90 days median2013: 88 days median2014: 124 days median2015: 102 days median2016: 121 days median2017: 67 days median2018: 95 days median2019: 81 days median2020: 55 days median2021: 59 days median2022: 85 days median2023: 59 days median2024: 64 days median2025: 64 days median2026 (partial year): 76 days median
2007high 124 (2014) · low 55 (2020)2026

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

Recalls per year · KWQ

1in 2018

2007: 22008: 332009: 352010: 22011: 52012: 72013: 62015: 22016: 92017: 82018: 1
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

2007: 2882008: 3482009: 3552010: 6912011: 4152012: 5442013: 7962014: 5462015: 5622016: 5022017: 4922018: 3412019: 2982020: 4002021: 5912022: 3922023: 3202024: 4192025: 248
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
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007271012288
2008327033348
2009239035355
2010231042691
201122955415
201226907544
201322886796
2014171240546
2015251022562
2016151219502
201720678492
201822951341
201926810298
202026550400
202117590591
202218850392
202316590320
202417640419
20257640248
202610760—

What is it indicated for?

The Anterior Cervical Plate System is intended for anterior screw fixation to the cervical spine. It is to be used in skeletally mature patients as an adjunct to fusion of the cervical spine (C2 to T1). The system is indicated for use in the temporary stabilization of the anterior spine during the development of cervical spinal fusion in patients with: • degenerative disc disease (as defined by neck pain of discogenic origin with degeneration of the disc…

Read the full statement (111 words)

The Anterior Cervical Plate System is intended for anterior screw fixation to the cervical spine. It is to be used in

skeletally mature patients as an adjunct to fusion of the cervical spine (C2 to T1). The system is indicated for use in the

temporary stabilization of the anterior spine during the development of cervical

spinal fusion in patients with:

• degenerative disc disease (as defined by neck pain of discogenic origin with degeneration of the disc confirmed by

patient history and radiographic studies),

• spondylolisthesis,

• trauma (i.e. fractures or dislocations),

• tumors,

• deformity (defined as kyphosis, lordosis, or scoliosis),

• pseudarthrosis,

• failed previous fusion,

• spinal stenosis

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K151553: Anterior 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/K151553

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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