510(k) Report

510(k) · Cleared

Cleared

Modification to Blackstone Spinal Fixation System

K030241510(k) SpecialCleared Feb 21, 200329-day reviewClass II21 CFR 888.3050

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

Blackstone Medical, Inc. · KWP Appliance, Fixation, Spinal Interlaminal

Cleared on Feb 21, 2003 as substantially equivalent to K994217 (Blackstone Medical, Inc., 2000) and 7 other predicates after a 29-day review. Its family tree reaches back 3 generations to 1998. 297 later devices descend from it.

Decided
Feb 21, 2003
Review
29 days
Class
Class II
Product code
KWP
Recalls
None
Predicates
8

Its longest line of descent runs back 3 generations to K980447 (1998). 11 ancestors in all. 297 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2002: 4 other ancestors2001: 1 other ancestor2000: 1 other ancestor1999: 1 other ancestor1998: 1 other ancestor2008: 3 descendants cleared2017: 23 descendants cleared2010: 4 descendants cleared2015: 9 descendants cleared2021: 16 descendants cleared2014: 5 descendants cleared2013: 9 descendants cleared2009: 1 descendant cleared2012: 5 descendants cleared2016: 12 descendants cleared2018: 16 descendants cleared2020: 23 descendants cleared2023: 36 descendants cleared2019: 17 descendants cleared2025: 34 descendants cleared2011: 2 descendants cleared2024: 33 descendants cleared2022: 23 descendants cleared2026: 26 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. · 20021995200020052010201520202025
Other ancestors, by generationDescendants, by generation 1 generation back: 6 other ancestors2 generations back: 2 other ancestors 1 generation forward: 1 descendant2 generations forward: 8 descendants3 generations forward: 22 descendants4 generations forward: 45 descendants5 generations forward: 59 descendants6 generations forward: 45 descendants7 generations forward: 41 descendants8 generations forward: 27 descendants9 generations forward: 8 descendants10 generations forward: 10 descendants11 generations forward: 16 descendants12 generations forward: 14 descendants13 generations forward: 1 descendant K022399 · 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. · 19980+5+10
  1. Root · 3 generations backK980447 Depuy Motech Moss Miami Spinal SystemDePuy Orthopaedics, Inc. · 1998
  2. 2 generations backK013558 Blackstone Spinal Fixation System 4.5MM Mono-Axial ScrewBlackstone Medical, Inc. · 2002
  3. 1 generation backK022399 Blackstone Spinal Fixation System SpacerBlackstone Medical, Inc. · 2002
  4. This deviceK030241 Modification to Blackstone Spinal Fixation SystemBlackstone Medical, Inc. · 2003
  5. Descendant · cites it directly · 296 of its ownK080407 Blackstone SFS Parallel Rod ConnectorsBlackstone Medical, Inc. · 2008 · Recalled
  6. Descendant · 2 generations on · 277 of its ownK081684 Blackstone Pedicle Screw SystemBlackstone Medical, Inc. · 2008 · Recalled
  7. Descendant · 3 generations on · 209 of its ownK082797 Blackstone Pedicle Screw SystemBlackstone Medical, Inc. · 2008
  8. Descendant · 3 generations on · 130 of its ownK092624 Firebird Spinal Fixation SystemBlackstone Medical, Inc. · 2009 · Recalled
  9. Descendant · 2 generations on · 117 of its ownK100044 Firebird Spinal Fixation System, Firebird Side-Loading BodyBlackstone · 2010

Showing 5 of 297 descendants. See all descendants

Descendants cleared per year

2008: 32009: 12010: 42011: 22012: 52013: 92014: 52015: 92016: 122017: 232018: 162019: 172020: 232021: 162022: 232023: 362024: 332025: 342026: 26
2008high 36 (2023) · low 1 (2009)2026

Most influential descendants

Showing 5 of 297 · See all
  • K080407Blackstone SFS Parallel Rod ConnectorsBlackstone Medical, Inc. · 2008 · cites it directly296descendants
  • K081684Blackstone Pedicle Screw SystemBlackstone Medical, Inc. · 2008 · 2 generations on277descendants
  • K082797Blackstone Pedicle Screw SystemBlackstone Medical, Inc. · 2008 · 3 generations on209descendants
  • K092624Firebird Spinal Fixation SystemBlackstone Medical, Inc. · 2009 · 3 generations on130descendants
  • K100044Firebird Spinal Fixation System, Firebird Side-Loading BodyBlackstone · 2010 · 2 generations on117descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K980447Depuy Motech Moss Miami Spinal SystemDePuy Orthopaedics, Inc.1998—
−2K013558Blackstone Spinal Fixation System 4.5MM Mono-Axial ScrewBlackstone Medical, Inc.2002—
−1K022399Blackstone Spinal Fixation System SpacerBlackstone Medical, Inc.2002—
0 (this device)K030241Modification to Blackstone Spinal Fixation SystemBlackstone Medical, Inc.2003—
+1K080407Blackstone SFS Parallel Rod ConnectorsBlackstone Medical, Inc.20081
+2K081684Blackstone Pedicle Screw SystemBlackstone Medical, Inc.20083
+3K082797Blackstone Pedicle Screw SystemBlackstone Medical, Inc.2008—
+3K092624Firebird Spinal Fixation SystemBlackstone Medical, Inc.20091
+2K100044Firebird Spinal Fixation System, Firebird Side-Loading BodyBlackstone2010—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199810
199910
200010
200110
200240

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200830
200910
201040
201120
201250
201390
201450
201590
2016120
2017230
2018160
2019170
2020230
2021160
2022230
2023360
2024330
2025340
2026260
FIG. 1 — Lineage of K030241, 1998–2026Source: 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 KWP? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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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
*K994217Blackstone Spinal Fixation System
Summary page 1
…l System KWP - 888.3050 - Spinal Interlaminal Fixation Orthosis Substantially Equivalent Devices: BlackstoneTMSpinal Fixation System (K9942 17) BlackstoneTMSpinal Fixation System 4.5mm Multi-Axial Screws (K020674) BlackstoneTMSpinal Fixation System 4.5mm Mono-…
Blackstone Medical, Inc.2000—
*K020674Blackstone Spinal Fixation System 4.5MM Multi-Axial Screw
Summary page 1
…xation Orthosis Substantially Equivalent Devices: BlackstoneTMSpinal Fixation System (K9942 17) BlackstoneTMSpinal Fixation System 4.5mm Multi-Axial Screws (K020674) BlackstoneTMSpinal Fixation System 4.5mm Mono-Axial Screws (KO13558) BlackstoneTMSpinal Fixation System 2nd Gen. Cro…
Blackstone Medical, Inc.2002—
*K013558Blackstone Spinal Fixation System 4.5MM Mono-Axial ScrewBlackstone Medical, Inc.2002—
*K003735Blackstone Spinal Fixation System, Second-Generation Cross-Connector
Summary page 1
…ulti-Axial Screws (K020674) BlackstoneTMSpinal Fixation System 4.5mm Mono-Axial Screws (KO13558) BlackstoneTMSpinal Fixation System 2nd Gen. Cross-Connector (K003735) BlackstoneTMSpinal Fixation System Modified Multi-Axial Screws (K023498) BlackstoneTMSpinal Fixation System Hooks (K…
Blackstone Medical, Inc.2001—
*K023498Modification to Blackstone Spinal Fixation System
Summary page 1
…-Axial Screws (KO13558) BlackstoneTMSpinal Fixation System 2nd Gen. Cross-Connector (K003735) BlackstoneTMSpinal Fixation System Modified Multi-Axial Screws (K023498) BlackstoneTMSpinal Fixation System Hooks (KO13885) BlackstoneTMSpinal Fixation System Spacers (K022399) Blacks…
Blackstone Medical, Inc.2002—
*K013885Blackstone Spinal Fixation System Posterior HooksBlackstone Medical, Inc.2002—
*K022399Blackstone Spinal Fixation System Spacer
Summary page 1
…TMSpinal Fixation System Modified Multi-Axial Screws (K023498) BlackstoneTMSpinal Fixation System Hooks (KO13885) BlackstoneTMSpinal Fixation System Spacers (K022399) BlackstoneTMSpinal Fixation System Staple & Washer (K022605) Device Description: The BlackstoneTMSpinal Fixation System…
Blackstone Medical, Inc.2002—
*K022605Blackstone Spinal Fixation System Staple & Washer
Summary page 1
…BlackstoneTMSpinal Fixation System Hooks (KO13885) BlackstoneTMSpinal Fixation System Spacers (K022399) BlackstoneTMSpinal Fixation System Staple & Washer (K022605) Device Description: The BlackstoneTMSpinal Fixation System is comprised of titanium alloy (GAL-4V ELI, per ASTM F136) devices…
Blackstone Medical, Inc.2002—
*—Danek device
Named without a submission number
—

Also cleared against K994217: 9 other devices →

What descends from it? (297)

See all 297

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

NumberDeviceApplicantDecidedDescendants
K080407Blackstone SFS Parallel Rod ConnectorsBlackstone Medical, Inc.2008296

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 5 years and passes through 2 companies; a new generation was cleared every 7 months on median.
  • None of the 11 ancestors has a recall.
  • Of its descendants, K080407 (Blackstone Medical, Inc., 2008) has gone furthest, with 296 descendants of its own.
  • 9 other devices also cite its predicate K994217.

How does its category compare?

All KWP devices

KWP Appliance, Fixation, Spinal Interlaminal: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KWP

9in 2015

2007: 142008: 132009: 122010: 142011: 122012: 182013: 122014: 132015: 9
2007high 18 (2012) · low 0 (2016)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KWP

113in 2015

2007: 96 days median2008: 50 days median2009: 89 days median2010: 186 days median2011: 67 days median2012: 112 days median2013: 99 days median2014: 138 days median2015: 113 days median
2007high 186 (2010) · low 50 (2008)2026

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

Recalls per year · KWP

2in 2022

2007: 22008: 12009: 232010: 22011: 62012: 12013: 32015: 12016: 32018: 12019: 22022: 2
2007high 23 (2009) · low 0 (2014)2026

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

Adverse event reports per year · KWP

494in 2025

2007: 2102008: 5942009: 6822010: 4742011: 7922012: 9182013: 1,0902014: 1,0222015: 1,3482016: 1,3792017: 8642018: 6572019: 5182020: 7962021: 5252022: 3352023: 3322024: 4362025: 494
2007high 1,379 (2016) · low 210 (2007)2025

MAUDE reports naming product code KWP, 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
200714962210
200813501594
2009128923682
2010141862474
201112676792
2012181121918
2013129931,090
20141313801,022
2015911311,348
20160—31,379
20170—0864
20180—1657
20190—2518
20200—0796
20210—0525
20220—2335
20230—0332
20240—0436
20250—0494
20260—0—

What is it indicated for?

The Blackstone Spinal Fixation System is intended for non-cervical use in the spine. The Blackstone Spinal Fixation System, when used for pedicle screw fixation, is intended only for patients: a) Having severe spondylolisthesis (Grades 3 and 4) at the L5-S1 joint; b) Who are receiving fusion using autogenous bone graft only; c) Who are having the device fixed or attached to the lumbar and sacral spine (L3 and below); and d) Who are having the device…

Read the full statement (298 words)

The Blackstone Spinal Fixation System is intended for non-cervical use in the spine.

The Blackstone Spinal Fixation System, when used for pedicle screw fixation, is intended only for patients:

a) Having severe spondylolisthesis (Grades 3 and 4) at the L5-S1 joint;

b) Who are receiving fusion using autogenous bone graft only;

c) Who are having the device fixed or attached to the lumbar and sacral spine (L3 and below); and

d) Who are having the device removed after the development of a solid fusion mass.

The Blackstone Spinal Fixation System, when used as a pedicle screw system in skeletally mature patients, is intended to provide immobilization and stabilization of spinal segments, as an adjunct to fusion, in treatment of the following acute and chronic instabilities or deformities of the thoracic, lumbar and sacral spine:

a) Degenerative spondylolistheses with objective evidence of neurologic impairment;

b) Fracture;

c) Dislocation;

d) Scoliosis;

e) Kyphosis;

f) Spinal tumor; and

g) Failed previous fusion (pseudarthrosis).

The Blackstone Spinal Fixation System, when used for anterolateral non'pedicle screw fixation to the non-cervical spine, is intended for the following indications:

a) Degenerative disc disease (as defined as back pain of discogenic origin with degenerative disc confirmed by history and radiographic studies);

b) spondylolistheses;

c) spinal stenosis;

d) spinal deformities (Le., scoliosis, kyphosis, lordosis);

e) tumor;

f) pseudoarthrosis;

g) previous failed fusion; and

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

The Blackstone Spinal Fixation System, when used for fixation system of the non-cervical spine, is intended for the following indications:

a) Degenerative disc disease (as defined as back pain of discogenic origin with degenerative disc confirmed by history and radiographic studies);

b) spondylolistheses;

c) spinal stenosis;

d) spinal deformities (i.e., scoliosis, kyphosis, lordosis);

e) tumor;

f) pseudoarthrosis;

g) previous failed fusion; and

h) trauma @e., fracture or dislocation).

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K030241: Modification to Blackstone Spinal Fixation System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K030241

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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