510(k) Report

510(k) · Cleared

Cleared

MSFX Mikron Peek Cages

K252781510(k) TraditionalCleared Dec 19, 2025108-day reviewClass II21 CFR 888.3080

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

Mikron Makina Sanayi VE Tic. Ltd. Sti. · ODP Intervertebral Fusion Device With Bone Graft, Cervical

Cleared on Dec 19, 2025 as substantially equivalent to K240893 (Artfx Medical, 2024) and 6 other predicates after a 108-day review. Its family tree reaches back 28 generations to 1984. 1 of the 543 devices in its family, counting itself, has a Class I recall. 1 later device descends from it.

Decided
Dec 19, 2025
Review
108 days
Class
Class II
Product code
ODP
Recalls
None
Predicates
7

Its longest line of descent runs back 28 generations to K841189 (1984). 541 ancestors in all, the oldest K792352 (1979). 1 later device descends from it, 1 citing it directly. 1 of the 543 devices in this family, counting this one, has a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 2024: 1 other ancestor2021: 1 other ancestor2018: 5 other ancestors2016: 9 other ancestors2017: 10 other ancestors2015: 20 other ancestors2014: 25 other ancestors2013: 26 other ancestors2012: 24 other ancestors2007: 22 other ancestors2020: 1 other ancestor2011: 34 other ancestors2010: 25 other ancestors2009: 35 other ancestors2008: 58 other ancestors, 1 with a Class I recall12006: 19 other ancestors2003: 26 other ancestors2002: 17 other ancestors2001: 19 other ancestors1999: 8 other ancestors1997: 10 other ancestors1993: 5 other ancestors2019: 1 other ancestor2005: 29 other ancestors2004: 34 other ancestors2000: 14 other ancestors1998: 7 other ancestors1996: 7 other ancestors1995: 5 other ancestors1988: 1 other ancestor1980: 1 other ancestor1979: 1 other ancestor1994: 2 other ancestors1992: 8 other ancestors1990: 3 other ancestors2026: 1 descendant clearedK841189 · Oec/Rezaian Spinal Fixator · Orthopedic Equipment Co., Inc. · 1984K990148 · Stackable Cage System · Depuy Motech Acromed · 1999K003043 · Surgical Titanium Mesh System · Depuyacromed · 2001×2: 2 generations cleared close together, K022793 (2003), K031757 (2003) ×2: 2 generations cleared close together, K041888 (2004), K042930 (2004) K062759 · Paramount VBR System · Innovative Spinal Technologies, Inc. · 2007×2: 2 generations cleared close together, K072120 (2007), K073291 (2008) K094025 · Crescent Spinal System · Medtronic Sofamor Danek · 2010K110543 · Crescent (R) Spinal System Titanium · Medtronic Sofamor Danek USA, Inc. · 2011×2: 2 generations cleared close together, K121683 (2012), K123752 (2013) K132505 · Acculif TL and PL Cage · Coalign Innovations, Inc. · 2013 · recalled×2: 2 generations cleared close together, K141217 (2014), K143163 (2015) ×2: 2 generations cleared close together, K153782 (2016), K161230 (2016) ×2: 2 generations cleared close together, K170962 (2017), K171633 (2017) ×4: 4 generations cleared close together, K180480 (2018), K181453 (2018), K182746 (2018), K183705 (2019) K202812 · IdentiTi Cervical Standalone Interbody System · Alphatec Spine, Inc. · 2020K212358 · Romero Cervical Cage · Spineup, Inc. · 2022K240893 · ARTFX MEDICAL Cervical PEEK Cages · Artfx Medical · 202419801990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 5 other ancestors2 generations back: 19 other ancestors3 generations back: 49 other ancestors4 generations back: 69 other ancestors, 1 with a Class I recall15 generations back: 117 other ancestors6 generations back: 97 other ancestors7 generations back: 77 other ancestors8 generations back: 52 other ancestors9 generations back: 19 other ancestors10 generations back: 4 other ancestors11 generations back: 4 other ancestors12 generations back: 1 other ancestor 1 generation forward: 1 descendant K240893 · ARTFX MEDICAL Cervical PEEK Cages · Artfx Medical · 2024K212358 · Romero Cervical Cage · Spineup, Inc. · 2022K202812 · IdentiTi Cervical Standalone Interbody System · Alphatec Spine, Inc. · 2020K183705 · IdentiTi Porous Ti Interbody System · Alphatec Spine, Inc. · 2019K182746 · ATEC ALIF and LLIF Spacer System · Alphatec Spine, Inc. · 2018K181453 · ATEC ALIF Spacer System · Alphatec Spine, Inc. · 2018K180480 · ATEC Universal Spacer System · Alphatec Spine, Inc. · 2018K171633 · NuVasive TLX Interbody System · Nu Vasive, Incorporated · 2017K170962 · NuVasive® CoRoent® Thoracolumbar System · Nu Vasive, Incorporated · 2017K161230 · NuVasive Lumbar Interbody Implants · Nu Vasive, Incorporated · 2016K153782 · NuVasive® Lumbar Interbody Implants · Nu Vasive, Incorporated · 2016K143163 · AVS® AL and ALign PEEK Spacers, AVS® PL and UniLIF PEEK Spacers, AVS® TL PEEK Spacer, AVS® Navigator PEEK Spacer, AVS® ARIA PEEK Spacer, AccuLIF TL and PL Cage, AVS® Anchor-L Spacer, Aero-AL Lumbar Cage System · Stryker Corporation · 2015K141217 · Acculif TL and PL Cage · Stryker Corporation · 2014 · recalledK132505 · Acculif TL and PL Cage · Coalign Innovations, Inc. · 2013 · recalledK123752 · Acculif TL and PL Cage · Coalign Innovations, Inc. · 2013K121683 · Acculif TL Cage · Coalign Innovations, Inc. · 2012K110543 · Crescent (R) Spinal System Titanium · Medtronic Sofamor Danek USA, Inc. · 2011K094025 · Crescent Spinal System · Medtronic Sofamor Danek · 2010K073291 · Capstone Spinal System · Medtronic Sofamor Danek USA, Inc. · 2008K072120 · Paramount Intervertebral Body Fusion Device · Innovative Spinal Technologies, Inc. · 2007K062759 · Paramount VBR System · Innovative Spinal Technologies, Inc. · 2007K042930 · Spacevision Cage System · Spine Vision, Inc. · 2004K041888 · Curved Peek Tetris Spinal Implant · Signus Medizintechnik GmbH · 2004K031757 · Peek Tetris Spinal Implant · Signus Medical, LLC · 2003K022793 · Tetris Spinal Implant · Signus Medical, LLC · 2003K003043 · Surgical Titanium Mesh System · Depuyacromed · 2001K990148 · Stackable Cage System · Depuy Motech Acromed · 1999K841189 · Oec/Rezaian Spinal Fixator · Orthopedic Equipment Co., Inc. · 1984−25−20−15−10−50
  1. Root · 28 generations backK841189 Oec/Rezaian Spinal FixatorOrthopedic Equipment Co., Inc. · 1984
  2. 24 generations between
  3. 3 generations backK202812 IdentiTi Cervical Standalone Interbody SystemAlphatec Spine, Inc. · 2020
  4. 2 generations backK212358 Romero Cervical CageSpineup, Inc. · 2022
  5. 1 generation backK240893 ARTFX MEDICAL Cervical PEEK CagesArtfx Medical · 2024
  6. This deviceK252781 MSFX Mikron Peek CagesMikron Makina Sanayi VE Tic. Ltd. Sti. · 2025
  7. Descendant · cites it directly · 0 of its ownK260340 HC Biologics Osteopoint Peek Cages, HC Biologics Osteopoint Cervical…HC Biologics, LLC · 2026
Show all 28 generations
  1. Root · 28 generations backK841189 Oec/Rezaian Spinal FixatorOrthopedic Equipment Co., Inc. · 1984
  2. 27 generations backK990148 Stackable Cage SystemDepuy Motech Acromed · 1999
  3. 26 generations backK003043 Surgical Titanium Mesh SystemDepuyacromed · 2001
  4. 25 generations backK022793 Tetris Spinal ImplantSignus Medical, LLC · 2003
  5. 24 generations backK031757 Peek Tetris Spinal ImplantSignus Medical, LLC · 2003
  6. 23 generations backK041888 Curved Peek Tetris Spinal ImplantSignus Medizintechnik GmbH · 2004
  7. 22 generations backK042930 Spacevision Cage SystemSpine Vision, Inc. · 2004
  8. 21 generations backK062759 Paramount VBR SystemInnovative Spinal Technologies, Inc. · 2007
  9. 20 generations backK072120 Paramount Intervertebral Body Fusion DeviceInnovative Spinal Technologies, Inc. · 2007
  10. 19 generations backK073291 Capstone Spinal SystemMedtronic Sofamor Danek USA, Inc. · 2008
  11. 18 generations backK094025 Crescent Spinal SystemMedtronic Sofamor Danek · 2010
  12. 17 generations backK110543 Crescent (R) Spinal System TitaniumMedtronic Sofamor Danek USA, Inc. · 2011
  13. 16 generations backK121683 Acculif TL CageCoalign Innovations, Inc. · 2012
  14. 15 generations backK123752 Acculif TL and PL CageCoalign Innovations, Inc. · 2013
  15. 14 generations backK132505 Acculif TL and PL CageCoalign Innovations, Inc. · 2013 · Recalled
  16. 13 generations backK141217 Acculif TL and PL CageStryker Corporation · 2014 · Recalled
  17. 12 generations backK143163 AVS® AL and ALign PEEK Spacers, AVS® PL and UniLIF PEEK Spacers…Stryker Corporation · 2015
  18. 11 generations backK153782 NuVasive® Lumbar Interbody ImplantsNu Vasive, Incorporated · 2016
  19. 10 generations backK161230 NuVasive Lumbar Interbody ImplantsNu Vasive, Incorporated · 2016
  20. 9 generations backK170962 NuVasive® CoRoent® Thoracolumbar SystemNu Vasive, Incorporated · 2017
  21. 8 generations backK171633 NuVasive TLX Interbody SystemNu Vasive, Incorporated · 2017
  22. 7 generations backK180480 ATEC Universal Spacer SystemAlphatec Spine, Inc. · 2018
  23. 6 generations backK181453 ATEC ALIF Spacer SystemAlphatec Spine, Inc. · 2018
  24. 5 generations backK182746 ATEC ALIF and LLIF Spacer SystemAlphatec Spine, Inc. · 2018
  25. 4 generations backK183705 IdentiTi Porous Ti Interbody SystemAlphatec Spine, Inc. · 2019
  26. 3 generations backK202812 IdentiTi Cervical Standalone Interbody SystemAlphatec Spine, Inc. · 2020
  27. 2 generations backK212358 Romero Cervical CageSpineup, Inc. · 2022
  28. 1 generation backK240893 ARTFX MEDICAL Cervical PEEK CagesArtfx Medical · 2024
  29. This deviceK252781 MSFX Mikron Peek CagesMikron Makina Sanayi VE Tic. Ltd. Sti. · 2025

Class I recalls in this family

  • K073202 Ardis Spacer4 generations back · 2008

Most influential descendants

Showing 1 of 1 · See all
  • K260340HC Biologics Osteopoint Peek Cages, HC Biologics Osteopoint Cervical Peek Cages, HC…HC Biologics, LLC · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−28K841189Oec/Rezaian Spinal FixatorOrthopedic Equipment Co., Inc.1984—
−27K990148Stackable Cage SystemDepuy Motech Acromed1999—
−26K003043Surgical Titanium Mesh SystemDepuyacromed2001—
−25K022793Tetris Spinal ImplantSignus Medical, LLC2003—
−24K031757Peek Tetris Spinal ImplantSignus Medical, LLC2003—
−23K041888Curved Peek Tetris Spinal ImplantSignus Medizintechnik GmbH2004—
−22K042930Spacevision Cage SystemSpine Vision, Inc.2004—
−21K062759Paramount VBR SystemInnovative Spinal Technologies, Inc.2007—
−20K072120Paramount Intervertebral Body Fusion DeviceInnovative Spinal Technologies, Inc.2007—
−19K073291Capstone Spinal SystemMedtronic Sofamor Danek USA, Inc.2008—
−18K094025Crescent Spinal SystemMedtronic Sofamor Danek2010—
−17K110543Crescent (R) Spinal System TitaniumMedtronic Sofamor Danek USA, Inc.2011—
−16K121683Acculif TL CageCoalign Innovations, Inc.2012—
−15K123752Acculif TL and PL CageCoalign Innovations, Inc.2013—
−14K132505Acculif TL and PL CageCoalign Innovations, Inc.20133
−13K141217Acculif TL and PL CageStryker Corporation20143
−12K143163AVS® AL and ALign PEEK Spacers, AVS® PL and UniLIF PEEK Spacers, AVS® TL PEEK…Stryker Corporation2015—
−11K153782NuVasive® Lumbar Interbody ImplantsNu Vasive, Incorporated2016—
−10K161230NuVasive Lumbar Interbody ImplantsNu Vasive, Incorporated2016—
−9K170962NuVasive® CoRoent® Thoracolumbar SystemNu Vasive, Incorporated2017—
−8K171633NuVasive TLX Interbody SystemNu Vasive, Incorporated2017—
−7K180480ATEC Universal Spacer SystemAlphatec Spine, Inc.2018—
−6K181453ATEC ALIF Spacer SystemAlphatec Spine, Inc.2018—
−5K182746ATEC ALIF and LLIF Spacer SystemAlphatec Spine, Inc.2018—
−4K183705IdentiTi Porous Ti Interbody SystemAlphatec Spine, Inc.2019—
−3K202812IdentiTi Cervical Standalone Interbody SystemAlphatec Spine, Inc.2020—
−2K212358Romero Cervical CageSpineup, Inc.2022—
−1K240893ARTFX MEDICAL Cervical PEEK CagesArtfx Medical2024—
0 (this device)K252781MSFX Mikron Peek CagesMikron Makina Sanayi VE Tic. Ltd. Sti.2025—
+1K260340HC Biologics Osteopoint Peek Cages, HC Biologics Osteopoint Cervical Peek…HC Biologics, LLC2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197910
198010
198810
199030
199280
199350
199420
199550
199670
1997100
199870
199980
2000140
2001190
2002170
2003260
2004340
2005290
2006190
2007220
2008581
2009350
2010250
2011340
2012240
2013260
2014250
2015200
201690
2017100
201850
201910
202010
202110
202410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202610
FIG. 1 — Lineage of K252781, 1984–2026Source: 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.

1 device in this family has a Class I recall. 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 ODP device

  1. #1 K222276 CONDUIT Cages; FIBERGRAFT BG Puttyscore 53.4 · 25 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? (7)

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
*K240893ARTFX MEDICAL Cervical PEEK Cages
Summary page 5
…Product Code(s) ODP, OVE, MAX I Legally Marketed Predicate Devices 21 CFR 807.92(a)(3) Predicate # Predicate Trade Name (Primary Predicate is listed first) Product Code K240893 ARTFX Medical Cervical PEEK Cages ODP K240889 ARTFX Lumbar PEEK Cages MAX K180078 Px® PEEK IBF System, Px HA® PEEK IBF System, Tx…
Artfx Medical2024—
*K240889ARTFX Lumbar PEEK Cages
Summary page 5
…ted Predicate Devices 21 CFR 807.92(a)(3) Predicate # Predicate Trade Name (Primary Predicate is listed first) Product Code K240893 ARTFX Medical Cervical PEEK Cages ODP K240889 ARTFX Lumbar PEEK Cages MAX K180078 Px® PEEK IBF System, Px HA® PEEK IBF System, TxHA™ MAX PEEK IBF System K172941 Cascadia Lat…
Artfx Medical2024—
*K180078Px PEEK IBF System, Px HA PEEK IBF System, TxHA PEEK IBF System
Summary page 5
…a)(3) Predicate # Predicate Trade Name (Primary Predicate is listed first) Product Code K240893 ARTFX Medical Cervical PEEK Cages ODP K240889 ARTFX Lumbar PEEK Cages MAX K180078 Px® PEEK IBF System, Px HA® PEEK IBF System, TxHA™ MAX PEEK IBF System K172941 Cascadia Lateral, K2M MAX K212266 FIX-C PEEK Ant…
Innovasis, Inc.20181
*K172941CASCADIA Interbody System
Summary page 5
…t Code K240893 ARTFX Medical Cervical PEEK Cages ODP K240889 ARTFX Lumbar PEEK Cages MAX K180078 Px® PEEK IBF System, Px HA® PEEK IBF System, TxHA™ MAX PEEK IBF System K172941 Cascadia Lateral, K2M MAX K212266 FIX-C PEEK Anterior Cervical Interbody System ODP K212358 ROMERO CERVICAL CAGE ODP K152011 Luce…
K2m2018—
*K212266FIX-C PEEK Anterior Cervical Interbody System
Summary page 5
…cal PEEK Cages ODP K240889 ARTFX Lumbar PEEK Cages MAX K180078 Px® PEEK IBF System, Px HA® PEEK IBF System, TxHA™ MAX PEEK IBF System K172941 Cascadia Lateral, K2M MAX K212266 FIX-C PEEK Anterior Cervical Interbody System ODP K212358 ROMERO CERVICAL CAGE ODP K152011 Lucent® Intervertebral Body Fusion Dev…
Jeil Medical Corporation2021—
*K212358Romero Cervical Cage
Summary page 5
…0078 Px® PEEK IBF System, Px HA® PEEK IBF System, TxHA™ MAX PEEK IBF System K172941 Cascadia Lateral, K2M MAX K212266 FIX-C PEEK Anterior Cervical Interbody System ODP K212358 ROMERO CERVICAL CAGE ODP K152011 Lucent® Intervertebral Body Fusion Device MAX Device Description Summary 21 CFR 807.92(a)(4) Th…
Spineup, Inc.2022—
*K152011Lucent Intervertebral Body Fusion Device
Summary page 5
…PEEK IBF System, TxHA™ MAX PEEK IBF System K172941 Cascadia Lateral, K2M MAX K212266 FIX-C PEEK Anterior Cervical Interbody System ODP K212358 ROMERO CERVICAL CAGE ODP K152011 Lucent® Intervertebral Body Fusion Device MAX Device Description Summary 21 CFR 807.92(a)(4) The MSFX Mikron Peek Cages are inte…
Spinal Elements, Inc.2016—

Also cleared against K240893: 1 other device →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K260340HC Biologics Osteopoint Peek Cages, HC Biologics Osteopoint Cervical Peek Cages, HC…HC Biologics, LLC20260

Has anything in its family been recalled? (1 Class I)

No FDA recall names this device.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

  • K073202Ardis SpacerAbbott Spine, Inc. · 2008 · 4 generations back · ◆ in the 2008 ancestors bar of FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 41 years and passes through 16 companies; a new generation was cleared every 10 months on median.
  • 66 of the 541 ancestors have a recall of any class; 1 has a Class I recall.
  • Of its descendants, K260340 (HC Biologics, LLC, 2026) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K240893.

How does its category compare?

All ODP devices

ODP Intervertebral Fusion Device With Bone Graft, Cervical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, this device’s year, is highlighted.

FDA decisions per year · ODP

11in 2025

2008: 82009: 122010: 92011: 252012: 172013: 182014: 262015: 242016: 172017: 332018: 252019: 222020: 142021: 182022: 122023: 342024: 102025: 112026 (partial year): 19
2007high 34 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ODP

87in 2025

2008: 89 days median2009: 127 days median2010: 151 days median2011: 113 days median2012: 93 days median2013: 187 days median2014: 118 days median2015: 180 days median2016: 112 days median2017: 104 days median2018: 133 days median2019: 92 days median2020: 89 days median2021: 121 days median2022: 92 days median2023: 165 days median2024: 76 days median2025: 87 days median2026 (partial year): 117 days median
2007high 187 (2013) · low 76 (2024)2026

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

Recalls per year · ODP

2in 2025

2009: 12011: 12013: 12020: 12025: 2
2007high 2 (2025) · low 0 (2007)2026

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

Adverse event reports per year · ODP

57in 2025

2008: 22009: 212010: 542011: 382012: 922013: 782014: 432015: 512016: 372017: 392018: 512019: 1412020: 862021: 1612022: 502023: 362024: 552025: 57
2007high 161 (2021) · low 0 (2007)2025

MAUDE reports naming product code ODP, 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
20070—00
200888902
200912127121
20109151054
201125113138
20121793092
201318187178
201426118043
201524180051
201617112037
201733104039
201825133051
201922920141
20201489186
2021181210161
20221292050
202334165036
20241076055
20251187257
2026191170—

What is it indicated for?

MSFX Mikron Cervical PEEK Cages are made to be implanted into the appropriate vertebral section to help provide stability for spinal fusion after a diseased cervical disc producing neck and/or armpain is removed during spinal decompression for patients who have had six weeks of non-operative treatment.Cervical PEEK Cages are indicated for use in skeletally mature patients with degenerative discdisease (DOD) of the cervical spine with accompanying…

Read the full statement (224 words)

MSFX Mikron Cervical PEEK Cages are made to be implanted into the appropriate vertebral section to help provide stability for spinal fusion after a diseased cervical disc producing neck and/or armpain is removed during spinal decompression for patients who have had six weeks of non-operative treatment.Cervical PEEK Cages are indicated for use in skeletally mature patients with degenerative discdisease (DOD) of the cervical spine with accompanying radicular symptoms at one disc level(C2-T1 ). DOD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies.Cervical PEEK Cages facilitate intervertebral body fusion in the cervical spine and are placed via the anterior approach and implanted with auto graft/autologous bone graft. They are to be used with supplemental fixation.

MSFX Mikron Lumbar PEEK Cages are indicated for intervertebral body fusion at one or two contiguous levels in the lumbar spine from L2 to S1 in skeletally mature patients with degenerative disc disease (ODD) of lumbar spine with up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s).Degenerative disc disease is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. Patients should have received at least six (6) months of prior non-operative treatment.The devices are designed to be used with supplemental fixation and autograft/autologous bone graft to facilitate fusion for each spinal region.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Also cleared against K240893

1 other device cites the same predicate.

  • K252686EffortMed PEEK Cages & Corpectomy CagesEffortmed, LLC · 2025

Recent decisions in ODP

The ODP category page

  • K262595VariLift-C Cervical Interbody Fusion SystemWenzel Spine, Inc. · 2026
  • K262489BluEX Cervical Expandable Cage SystemL&K BIOMED Co., Ltd. · 2026
  • K2530413d Cage CervicalFims Co., Ltd. · 2026
  • K262061Tritanium® C Anterior Cervical Cage; Tritanium® PL Cage; Tritanium® TL Curved Posterior Lumbar Cage; Aero®…Stryker Spine · 2026
  • K254130C.A. Medical Interbody Fusion SystemC.A. Medical, LLC · 2026

https://510kreport.com/device/K252781 · printed Nov 6, 2026

Cite this page

510(k) Report. “K252781: MSFX Mikron Peek Cages.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K252781

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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