510(k) Report

510(k) · Cleared

Cleared

MASADA Modular Spinal Fixation System

K231694510(k) TraditionalCleared Nov 16, 2023160-day reviewClass II21 CFR 888.3070

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

Astura Medical · NKB Thoracolumbosacral Pedicle Screw System

Cleared on Nov 16, 2023 as substantially equivalent to K181139 (Astura Medical, LLC, 2018) and 3 other predicates after a 160-day review. Its family tree reaches back 18 generations to 2004. 1 of the 406 devices in its family, counting itself, has a Class I recall. 2 later devices descend from it.

Decided
Nov 16, 2023
Review
160 days
Class
Class II
Product code
NKB
Recalls
None
Predicates
4

Its longest line of descent runs back 18 generations to K040583 (2004). 403 ancestors in all, the oldest K781443 (1978). 2 later devices descend from it, 2 citing it directly. 1 of the 406 devices in this family, counting this one, has a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 2023: 1 other ancestor2018: 2 other ancestors2013: 10 other ancestors2017: 3 other ancestors2016: 5 other ancestors2015: 6 other ancestors2014: 7 other ancestors2012: 11 other ancestors2011: 11 other ancestors2010: 16 other ancestors, 1 with a Class I recall12009: 16 other ancestors2007: 18 other ancestors2006: 23 other ancestors2003: 22 other ancestors2000: 22 other ancestors1997: 12 other ancestors1996: 6 other ancestors1995: 13 other ancestors1992: 8 other ancestors2008: 22 other ancestors2005: 26 other ancestors2004: 26 other ancestors2002: 21 other ancestors2001: 25 other ancestors1999: 12 other ancestors1993: 5 other ancestors1990: 3 other ancestors1998: 15 other ancestors1994: 6 other ancestors1978: 1 other ancestor1988: 3 other ancestors1987: 1 other ancestor1984: 2 other ancestors1989: 1 other ancestor1986: 2 other ancestors1985: 2 other ancestors2025: 2 descendants cleared×7: 7 generations cleared close together, K040583 (2004), K041118 (2004), K042025 (2004), K043151 (2005), K050809 (2005), K052187 (2005), K053101 (2006) ×2: 2 generations cleared close together, K091442 (2009), K091974 (2009) K102555 · CD Horizon Spinal System · Medtronic Sofamor Danek USA, Inc. · 2010×2: 2 generations cleared close together, K112473 (2011), K113174 (2011) K121680 · CD Horizon Spinal System · Medtronic Sofamor Danek USA, Inc. · 2012×3: 3 generations cleared close together, K131321 (2013), K132471 (2013), K140276 (2014) K142381 · Xia 3 Spinal System · Stryker Corp. · 2014K181139 · OLYMPIC Posterior Spinal Fixation System · Astura Medical, LLC · 201819801990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 3 other ancestors2 generations back: 28 other ancestors, 1 with a Class I recall13 generations back: 67 other ancestors4 generations back: 102 other ancestors5 generations back: 74 other ancestors6 generations back: 48 other ancestors7 generations back: 27 other ancestors8 generations back: 15 other ancestors9 generations back: 15 other ancestors10 generations back: 6 other ancestors 1 generation forward: 2 descendants K181139 · OLYMPIC Posterior Spinal Fixation System · Astura Medical, LLC · 2018K142381 · Xia 3 Spinal System · Stryker Corp. · 2014K140276 · CD Horizon Spinal System · Medtronic Sofamor Danek · 2014K132471 · CD Horizon Spinal System · Medtronic Sofamor Danek USA, Inc. · 2013K131321 · CD Horizon Spinal System · Medtronic Sofamor Danek USA · 2013K121680 · CD Horizon Spinal System · Medtronic Sofamor Danek USA, Inc. · 2012K113174 · CD Horizon Spinal System · Medtronic Sofamor Danek USA, Inc. · 2011 · recalledK112473 · CD Horizon Spinal System · Medtronic Sofamor Danek, Inc. · 2011K102555 · CD Horizon Spinal System · Medtronic Sofamor Danek USA, Inc. · 2010K091974 · Modification to CD Horizon Spinal System · Medtronic Sofamor Danek USA, Inc. · 2009 · recalledK091442 · CD Horizon Spinal System · Medtronic Sofamor Danek · 2009K053101 · CD Horizon Spinal System · Medtronic Sofamor Danek · 2006K052187 · Modification to: CD Horizon Spinal System · Medtronic Sofamor Danek · 2005K050809 · CD Horizon Spinal System · Medtronic Sofamor Danek USA, Inc. · 2005K043151 · Modification to: CD Horizon Spinal System · Medtronic Sofamor Danek · 2005K042025 · Modification to CD Horizon Spinal System · Medtronic Sofamor Danek, Inc. · 2004 · recalledK041118 · Modification to CD Horizon Spinal System · Medtronic Sofamor Danek · 2004K040583 · Modification to: CD Horizon Spinal System · Medtronic Sofamor Danek · 2004−15−10−50
  1. Root · 18 generations backK040583 Modification to: CD Horizon Spinal SystemMedtronic Sofamor Danek · 2004
  2. 14 generations between
  3. 3 generations backK140276 CD Horizon Spinal SystemMedtronic Sofamor Danek · 2014
  4. 2 generations backK142381 Xia 3 Spinal SystemStryker Corp. · 2014
  5. 1 generation backK181139 OLYMPIC Posterior Spinal Fixation SystemAstura Medical, LLC · 2018
  6. This deviceK231694 MASADA Modular Spinal Fixation SystemAstura Medical · 2023
  7. Descendant · cites it directly · 0 of its ownK252346 OLYMPIC Posterior Spinal Fixation System; MASADA Modular Spinal…Astura Medical · 2025
  8. Descendant · cites it directly · 0 of its ownK243259 MASADA Modular Spinal Fixation SystemAstura Medical · 2025
Show all 18 generations
  1. Root · 18 generations backK040583 Modification to: CD Horizon Spinal SystemMedtronic Sofamor Danek · 2004
  2. 17 generations backK041118 Modification to CD Horizon Spinal SystemMedtronic Sofamor Danek · 2004
  3. 16 generations backK042025 Modification to CD Horizon Spinal SystemMedtronic Sofamor Danek, Inc. · 2004 · Recalled
  4. 15 generations backK043151 Modification to: CD Horizon Spinal SystemMedtronic Sofamor Danek · 2005
  5. 14 generations backK050809 CD Horizon Spinal SystemMedtronic Sofamor Danek USA, Inc. · 2005
  6. 13 generations backK052187 Modification to: CD Horizon Spinal SystemMedtronic Sofamor Danek · 2005
  7. 12 generations backK053101 CD Horizon Spinal SystemMedtronic Sofamor Danek · 2006
  8. 11 generations backK091442 CD Horizon Spinal SystemMedtronic Sofamor Danek · 2009
  9. 10 generations backK091974 Modification to CD Horizon Spinal SystemMedtronic Sofamor Danek USA, Inc. · 2009 · Recalled
  10. 9 generations backK102555 CD Horizon Spinal SystemMedtronic Sofamor Danek USA, Inc. · 2010
  11. 8 generations backK112473 CD Horizon Spinal SystemMedtronic Sofamor Danek, Inc. · 2011
  12. 7 generations backK113174 CD Horizon Spinal SystemMedtronic Sofamor Danek USA, Inc. · 2011 · Recalled
  13. 6 generations backK121680 CD Horizon Spinal SystemMedtronic Sofamor Danek USA, Inc. · 2012
  14. 5 generations backK131321 CD Horizon Spinal SystemMedtronic Sofamor Danek USA · 2013
  15. 4 generations backK132471 CD Horizon Spinal SystemMedtronic Sofamor Danek USA, Inc. · 2013
  16. 3 generations backK140276 CD Horizon Spinal SystemMedtronic Sofamor Danek · 2014
  17. 2 generations backK142381 Xia 3 Spinal SystemStryker Corp. · 2014
  18. 1 generation backK181139 OLYMPIC Posterior Spinal Fixation SystemAstura Medical, LLC · 2018
  19. This deviceK231694 MASADA Modular Spinal Fixation SystemAstura Medical · 2023

Class I recalls in this family

Most influential descendants

Showing 2 of 2 · See all
  • K252346OLYMPIC Posterior Spinal Fixation System; MASADA Modular Spinal Fixation SystemAstura Medical · 2025 · cites it directly0descendants
  • K243259MASADA Modular Spinal Fixation SystemAstura Medical · 2025 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−18K040583Modification to: CD Horizon Spinal SystemMedtronic Sofamor Danek2004—
−17K041118Modification to CD Horizon Spinal SystemMedtronic Sofamor Danek2004—
−16K042025Modification to CD Horizon Spinal SystemMedtronic Sofamor Danek, Inc.20044
−15K043151Modification to: CD Horizon Spinal SystemMedtronic Sofamor Danek2005—
−14K050809CD Horizon Spinal SystemMedtronic Sofamor Danek USA, Inc.2005—
−13K052187Modification to: CD Horizon Spinal SystemMedtronic Sofamor Danek2005—
−12K053101CD Horizon Spinal SystemMedtronic Sofamor Danek2006—
−11K091442CD Horizon Spinal SystemMedtronic Sofamor Danek2009—
−10K091974Modification to CD Horizon Spinal SystemMedtronic Sofamor Danek USA, Inc.20091
−9K102555CD Horizon Spinal SystemMedtronic Sofamor Danek USA, Inc.2010—
−8K112473CD Horizon Spinal SystemMedtronic Sofamor Danek, Inc.2011—
−7K113174CD Horizon Spinal SystemMedtronic Sofamor Danek USA, Inc.20111
−6K121680CD Horizon Spinal SystemMedtronic Sofamor Danek USA, Inc.2012—
−5K131321CD Horizon Spinal SystemMedtronic Sofamor Danek USA2013—
−4K132471CD Horizon Spinal SystemMedtronic Sofamor Danek USA, Inc.2013—
−3K140276CD Horizon Spinal SystemMedtronic Sofamor Danek2014—
−2K142381Xia 3 Spinal SystemStryker Corp.2014—
−1K181139OLYMPIC Posterior Spinal Fixation SystemAstura Medical, LLC2018—
0 (this device)K231694MASADA Modular Spinal Fixation SystemAstura Medical2023—
+1K252346OLYMPIC Posterior Spinal Fixation System; MASADA Modular Spinal Fixation SystemAstura Medical2025—
+1K243259MASADA Modular Spinal Fixation SystemAstura Medical2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197810
198420
198520
198620
198710
198830
198910
199030
199280
199350
199460
1995130
199660
1997120
1998150
1999120
2000220
2001250
2002210
2003220
2004260
2005260
2006230
2007180
2008220
2009160
2010161
2011110
2012110
2013100
201470
201560
201650
201730
201820
202310

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202520
FIG. 1 — Lineage of K231694, 2004–2025Source: 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 NKB device

  1. #1 K223494 CD Horizon Spinal Systemscore 40.4 · 30 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? (4)

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
*K181139OLYMPIC Posterior Spinal Fixation System
Summary page 5
…21 CFR section 888.3070, 888.3050, 888.3010, 882.4560 Device Panel Orthopedic Primary Predicate Device OLYMPIC Posterior Spinal Fixation System (K181139) Additional Predicate OLYMPIC Navigated Instruments (K172166) Device(s) OLYMPIC Deformity Band System…
Astura Medical, LLC2018—
*K172166OLYMPIC Navigated Instruments
Summary page 5
…el Orthopedic Primary Predicate Device OLYMPIC Posterior Spinal Fixation System (K181139) Additional Predicate OLYMPIC Navigated Instruments (K172166) Device(s) OLYMPIC Deformity Band System (K222097) Globus CREO Stabilization Syst…
Astura Medical2018—
*K222097OLYMPIC Deformity Band System
Summary page 5
…sterior Spinal Fixation System (K181139) Additional Predicate OLYMPIC Navigated Instruments (K172166) Device(s) OLYMPIC Deformity Band System (K222097) Globus CREO Stabilization System (K124058) Device Description The MASADA Modular Spinal F…
Astura Medical2023—
*K124058Creo Stabilization System
Summary page 5
…YMPIC Navigated Instruments (K172166) Device(s) OLYMPIC Deformity Band System (K222097) Globus CREO Stabilization System (K124058) Device Description The MASADA Modular Spinal Fixation System is a top loading thoracolumb…
Globus Medical, Inc.2013—

Also cleared against K181139: 3 other devices →

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K252346OLYMPIC Posterior Spinal Fixation System; MASADA Modular Spinal Fixation SystemAstura Medical20250
K243259MASADA Modular Spinal Fixation SystemAstura Medical20250

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.

  • K100952Modification to Synthes Matrix SystemSynthes Spine · 2010 · 2 generations back · ◆ in the 2010 ancestors bar of FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 19 years and passes through 7 companies; a new generation was cleared every 5 months on median.
  • 43 of the 403 ancestors have a recall of any class; 1 has a Class I recall.
  • Of its descendants, K252346 (Astura Medical, 2025) has gone furthest, with 0 descendants of its own.
  • 3 other devices also cite its predicate K181139.

How does its category compare?

All NKB devices

NKB Thoracolumbosacral Pedicle Screw System: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · NKB

24in 2025

2007: 382008: 362009: 442010: 372011: 482012: 602013: 352014: 462015: 552016: 502017: 632018: 562019: 392020: 482021: 322022: 342023: 442024: 392025: 242026 (partial year): 30
2007high 63 (2017) · low 24 (2025)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NKB

61in 2025

2007: 87 days median2008: 59 days median2009: 71 days median2010: 111 days median2011: 84 days median2012: 79 days median2013: 73 days median2014: 90 days median2015: 90 days median2016: 84 days median2017: 69 days median2018: 61 days median2019: 84 days median2020: 68 days median2021: 61 days median2022: 88 days median2023: 72 days median2024: 57 days median2025: 61 days median2026 (partial year): 91 days median
2007high 111 (2010) · low 57 (2024)2026

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

Recalls per year · NKB

1in 2025

2007: 42008: 52009: 332010: 42011: 32012: 132014: 3, 1 Class I2015: 32016: 12017: 12018: 32019: 12020: 12022: 52023: 22024: 32025: 12026 (partial year): 3
2007high 33 (2009) · low 0 (2013)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · NKB

1,171in 2025

2007: 342008: 822009: 1712010: 4622011: 5772012: 1,7472013: 1,9622014: 1,6712015: 1,4462016: 1,5852017: 1,6182018: 1,6842019: 1,9152020: 2,0762021: 1,7452022: 1,3392023: 9192024: 1,6142025: 1,171
2007high 2,076 (2020) · low 34 (2007)2025

MAUDE reports naming product code NKB, 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
20073887434
20083659582
2009447133171
2010371114462
201148843577
20126079131,747
2013357301,962
201446903 (1)1,671
2015559031,446
2016508411,585
2017636911,618
2018566131,684
2019398411,915
2020486812,076
2021326101,745
2022348851,339
202344722919
2024395731,614
2025246111,171
202630913—

What is it indicated for?

Pedicle Screw System: The MASADA Modular Spinal Fixation System is intended for immobilization and stabilization of the posterior, non-cervical spine in skeletally mature patients as an adjunct to fusion for the following indications: degenerative disc disease ( defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), spinal stenosis…

Read the full statement (383 words)

Pedicle Screw System: The MASADA Modular Spinal Fixation System is intended for immobilization and stabilization of the posterior, non-cervical spine in skeletally mature patients as an adjunct to fusion for the following indications: degenerative disc disease ( defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), spinal stenosis, curvatures (i.e., scoliosis, kyphosis, or lordosis), tumor, pseudoarthrosis, and/or failed previous fusion.

When used for posterior non-cervical pedicle screw fixation in pediatric patients, the MASADA pedicle screw implants are indicated as an adjunct to fusion to treat adolescent idiopathic scoliosis. The MASADA pedicle screw is intended to be used with autograft and/or allograft. Pediatric pedicle screw fixation is limited to a posterior approach.

Navigated Instrument System: The MASADA navigated instruments are intended to be used in the preparation and placement of MASADA screws during spinal surgery to assist the surgeon in precisely locating anatomical structures in either open or minimally invasive procedures. These instruments are designed for use with the Medtronic StealthStation® System, which is indicated for any medical condition in which the use of stereotactic surgery may be appropriate, and where reference to a rigid anatomical structure, such as a skull, a long bone, or vertebra, can be identified relative to a CT or MR based model, fluoroscopy images, or digitized landmarks of the anatomy. Refer to the Astura Navigated Instrument system Instructions For Use (INS-00006) regarding the use of these instruments.

Sublaminar Band System: The MASADA sublaminar band is a temporary implant for use in orthopedic surgery. The band system is intended to provide temporary stabilization as a bone anchor during the development of solid bony fusion and aid in the repair of bone fractures. The indications for use include the following applications:

- Spinal trauma surgery, used in sublaminar or facet wiring techniques.

- Spinal reconstructive surgery, incorporated into constructs for the purpose of correction of spinal deformities such as idiopathic and neuromuscular scoliosis in patients 8 years of age or older, adult scoliosis, kyphosis and spondylolisthesis.

- Spinal degenerative surgery, as an adjunct to spinal fusions.

The MASADA sublaminar band may also be used in conjunction with other medical grade implants made of similar metals whenever "wiring" may help secure the attachment of the other implants.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K231694: MASADA Modular Spinal Fixation System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K231694

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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