510(k) Report

510(k) · Cleared

Recalled · 2011

Firebird Spinal Fixation System

K092624510(k) SpecialCleared Sep 25, 200930-day reviewClass II21 CFR 888.3070Recalls 1

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

Blackstone Medical, Inc. · NKB Thoracolumbosacral Pedicle Screw System

Cleared on Sep 25, 2009 as substantially equivalent to K081684 (Blackstone Medical, Inc., 2008) and 3 other predicates after a 30-day review. Its family tree reaches back 7 generations to 1998. 130 later devices descend from it. It has been recalled once.

Decided
Sep 25, 2009
Review
30 days
Class
Class II
Product code
NKB
Recalls
1
Predicates
4

Its longest line of descent runs back 7 generations to K980447 (1998). 58 ancestors in all, the oldest K901587 (1990). 130 later devices descend from it, 5 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2008: 1 other ancestor2006: 1 other ancestor2007: 1 other ancestor2005: 3 other ancestors2004: 4 other ancestors2003: 5 other ancestors2002: 4 other ancestors2001: 1 other ancestor2000: 2 other ancestors1999: 3 other ancestors1998: 5 other ancestors1997: 3 other ancestors1996: 4 other ancestors1995: 3 other ancestors1994: 2 other ancestors1993: 2 other ancestors1992: 5 other ancestors1990: 2 other ancestors2011: 1 descendant cleared2010: 2 descendants cleared2012: 1 descendant cleared2013: 4 descendants cleared2014: 2 descendants cleared2017: 11 descendants cleared2021: 9 descendants cleared2020: 8 descendants cleared2016: 6 descendants cleared2018: 7 descendants cleared2024: 11 descendants cleared2015: 4 descendants cleared2025: 14 descendants cleared2019: 9 descendants cleared2023: 15 descendants cleared2022: 13 descendants cleared2026: 13 descendants clearedK980447 · Depuy Motech Moss Miami Spinal System · DePuy Orthopaedics, Inc. · 1998K013558 · Blackstone Spinal Fixation System 4.5MM Mono-Axial Screw · Blackstone Medical, Inc. · 2002K022399 · Blackstone Spinal Fixation System Spacer · Blackstone Medical, Inc. · 2002K030241 · Modification to Blackstone Spinal Fixation System · Blackstone Medical, Inc. · 2003K080407 · Blackstone SFS Parallel Rod Connectors · Blackstone Medical, Inc. · 2008 · recalled×2: 2 generations cleared close together, K081684 (2008), K082797 (2008) 1990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 2 other ancestors2 generations back: 12 other ancestors3 generations back: 15 other ancestors4 generations back: 20 other ancestors5 generations back: 2 other ancestors 1 generation forward: 5 descendants2 generations forward: 10 descendants3 generations forward: 23 descendants4 generations forward: 27 descendants5 generations forward: 27 descendants6 generations forward: 28 descendants7 generations forward: 6 descendants8 generations forward: 3 descendants9 generations forward: 1 descendant K082797 · Blackstone Pedicle Screw System · Blackstone Medical, Inc. · 2008K081684 · Blackstone Pedicle Screw System · Blackstone Medical, Inc. · 2008 · recalledK080407 · Blackstone SFS Parallel Rod Connectors · Blackstone Medical, Inc. · 2008 · recalledK030241 · Modification to Blackstone Spinal Fixation System · Blackstone Medical, Inc. · 2003K022399 · Blackstone Spinal Fixation System Spacer · Blackstone Medical, Inc. · 2002K013558 · Blackstone Spinal Fixation System 4.5MM Mono-Axial Screw · Blackstone Medical, Inc. · 2002K980447 · Depuy Motech Moss Miami Spinal System · DePuy Orthopaedics, Inc. · 1998−50+5
  1. Root · 7 generations backK980447 Depuy Motech Moss Miami Spinal SystemDePuy Orthopaedics, Inc. · 1998
  2. 6 generations backK013558 Blackstone Spinal Fixation System 4.5MM Mono-Axial ScrewBlackstone Medical, Inc. · 2002
  3. 5 generations backK022399 Blackstone Spinal Fixation System SpacerBlackstone Medical, Inc. · 2002
  4. 4 generations backK030241 Modification to Blackstone Spinal Fixation SystemBlackstone Medical, Inc. · 2003
  5. 3 generations backK080407 Blackstone SFS Parallel Rod ConnectorsBlackstone Medical, Inc. · 2008 · Recalled
  6. 2 generations backK081684 Blackstone Pedicle Screw SystemBlackstone Medical, Inc. · 2008 · Recalled
  7. 1 generation backK082797 Blackstone Pedicle Screw SystemBlackstone Medical, Inc. · 2008
  8. This deviceK092624 Firebird Spinal Fixation SystemBlackstone Medical, Inc. · 2009
  9. Descendant · cites it directly · 117 of its ownK100044 Firebird Spinal Fixation System, Firebird Side-Loading BodyBlackstone · 2010
  10. Descendant · cites it directly · 116 of its ownK122901 Firebird Spinal Fixation System, Phoenix Mis Spinal Fixation SystemOrthofix · 2012
  11. Descendant · cites it directly · 88 of its ownK093926 Firebird Spinal Fixation SystemBlackstone Medical, Inc. · 2010
  12. Descendant · 2 generations on · 81 of its ownK130932 Firebird Spinal Fixation SystemOrthofix, Inc. · 2013 · Recalled
  13. Descendant · 3 generations on · 78 of its ownK151488 Firebird Spinal Fixation System/Phoenix MIS Spinal Fixation SystemOrthofix, Inc. · 2015 · Recalled

Showing 5 of 130 descendants. See all descendants

Descendants cleared per year

2010: 22011: 12012: 12013: 42014: 22015: 42016: 62017: 112018: 72019: 92020: 82021: 92022: 132023: 152024: 112025: 142026: 13
2010high 15 (2023) · low 1 (2011)2026

Most influential descendants

Showing 5 of 130 · See all
  • K100044Firebird Spinal Fixation System, Firebird Side-Loading BodyBlackstone · 2010 · cites it directly117descendants
  • K122901Firebird Spinal Fixation System, Phoenix Mis Spinal Fixation SystemOrthofix · 2012 · cites it directly116descendants
  • K093926Firebird Spinal Fixation SystemBlackstone Medical, Inc. · 2010 · cites it directly88descendants
  • K130932Firebird Spinal Fixation SystemOrthofix, Inc. · 2013 · 2 generations on81descendants
  • K151488Firebird Spinal Fixation System/Phoenix MIS Spinal Fixation SystemOrthofix, Inc. · 2015 · 3 generations on78descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K980447Depuy Motech Moss Miami Spinal SystemDePuy Orthopaedics, Inc.1998—
−6K013558Blackstone Spinal Fixation System 4.5MM Mono-Axial ScrewBlackstone Medical, Inc.2002—
−5K022399Blackstone Spinal Fixation System SpacerBlackstone Medical, Inc.2002—
−4K030241Modification to Blackstone Spinal Fixation SystemBlackstone Medical, Inc.2003—
−3K080407Blackstone SFS Parallel Rod ConnectorsBlackstone Medical, Inc.20081
−2K081684Blackstone Pedicle Screw SystemBlackstone Medical, Inc.20083
−1K082797Blackstone Pedicle Screw SystemBlackstone Medical, Inc.2008—
0 (this device)K092624Firebird Spinal Fixation SystemBlackstone Medical, Inc.2009—
+1K100044Firebird Spinal Fixation System, Firebird Side-Loading BodyBlackstone2010—
+1K122901Firebird Spinal Fixation System, Phoenix Mis Spinal Fixation SystemOrthofix2012—
+1K093926Firebird Spinal Fixation SystemBlackstone Medical, Inc.2010—
+2K130932Firebird Spinal Fixation SystemOrthofix, Inc.20131
+3K151488Firebird Spinal Fixation System/Phoenix MIS Spinal Fixation SystemOrthofix, Inc.20151

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199020
199250
199320
199420
199530
199640
199730
199850
199930
200020
200110
200240
200350
200440
200530
200610
200710
200810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201020
201110
201210
201340
201420
201540
201660
2017110
201870
201990
202080
202190
2022130
2023150
2024110
2025140
2026130
FIG. 1 — Lineage of K092624, 1998–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 NKB? 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
*K081684Blackstone Pedicle Screw System
Summary page 2
…II - 888.3070 - Pedicle Screw Spinal System Review Panel: Orthopedic Device Panel Predicate Devices: Blackstone Pedicle Screw System (K081684 SE 9/15/08) Blackstone Pedicle Screw System, 4.0 mm Screws (K08…
Blackstone Medical, Inc.20083
*K082797Blackstone Pedicle Screw System
Summary page 2
…Blackstone Pedicle Screw System (K081684 SE 9/15/08) Blackstone Pedicle Screw System, 4.0 mm Screws (K082797 SE 10/17/08) K2M, Inc. CoCr Rod (K080792 SE 4-8-08) Applied Spi…
Blackstone Medical, Inc.2008—
*K080792K2M Cocr Rod
Summary page 2
…Blackstone Pedicle Screw System, 4.0 mm Screws (K082797 SE 10/17/08) K2M, Inc. CoCr Rod (K080792 SE 4-8-08) Applied Spine Technologies, Inc. Bar Pedicle Screw Spinal…
K2m, Inc.2008—
*K061162Bar Pedicle Screw Spinal Fixation System, Model 2020
Summary page 2
…CoCr Rod (K080792 SE 4-8-08) Applied Spine Technologies, Inc. Bar Pedicle Screw Spinal Fixation System (K061162 SE 7-26-06) Intended Use / Indications for Use The Firebird Spinal Fixation System is intended for posterior, non-cervical pedi…
Applied Spine Technologies, Inc.2006—

Also cleared against K081684: 6 other devices →

What descends from it? (130)

See all 130

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

NumberDeviceApplicantDecidedDescendants
K100044Firebird Spinal Fixation System, Firebird Side-Loading BodyBlackstone2010117
K122901Firebird Spinal Fixation System, Phoenix Mis Spinal Fixation SystemOrthofix2012116
K093926Firebird Spinal Fixation SystemBlackstone Medical, Inc.201088
K111183Ascent Posterior Occipital Thoracic (Poct) System (Titanium & Cobalt Chrome Rods)Orthofix, Inc.201122
K132644Lospa IS Pedicle Screw (Monoaxial & Polyaxial), Lospa IS Rod- Straight (Standard), Lospa…Corentec Co., Ltd.20130

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Apr 1, 2011Not classifiedZ-3162-2011Device DesignUpon reaching torque limit, there is a possibility the product may jam or exhibit a ratchet direction switch from forward to reverse.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 11 years and passes through 2 companies; a new generation was cleared every 7 months on median.
  • 5 of the 58 ancestors have a recall of any class.
  • Of its descendants, K100044 (Blackstone, 2010) has gone furthest, with 117 descendants of its own.
  • 6 other devices also cite its predicate K081684.

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. 2009, 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?

The Firebird Spinal Fixation System is intended for posterior, non-cervical pedicle fixation. Pedicle screw fixation is limited to skeletally mature patients and is intended to be used as an adjunct to fusion using autograft or allograft. The device is indicated for all of the following indications: 1) degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies) 2)…

Read the full statement (117 words)

The Firebird Spinal Fixation System is intended for posterior, non-cervical pedicle fixation. Pedicle screw fixation is limited to skeletally mature patients and is intended to be used as an adjunct to fusion using autograft or allograft. The device is indicated for all of the following indications:

1) degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies)

2) spondylolisthesis,

3) trauma (i.e., fracture or dislocation),

4) spinal stenosis,

5) deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis),

6) tumor,

7) pseudoarthrosis, and

8) failed previous fusion

The Firebird Spinal Fixation System components are used with certain components of the Blackstone SFS system, including rods, rod connectors and cross-connectors.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K092624: Firebird Spinal Fixation System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K092624

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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