510(k) Report

510(k) · Cleared

Cleared

Silc Fixation System

K133482510(k) TraditionalCleared May 21, 2014189-day reviewClass II21 CFR 888.3010

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

Globus Medical, Inc. · OWI Bone Fixation Cerclage, Sublaminar

Cleared on May 21, 2014 as substantially equivalent to K060009 (Abbott Spine, Inc., 2006) and 3 other predicates after a 189-day review. Its family tree reaches back 6 generations to 1993. 11 later devices descend from it.

Decided
May 21, 2014
Review
189 days
Class
Class II
Product code
OWI
Recalls
None
Predicates
4

Its longest line of descent runs back 6 generations to K925812 (1993). 28 ancestors in all, the oldest K781443 (1978). 11 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2012: 1 other ancestor1993: 1 other ancestor2010: 1 other ancestor2000: 4 other ancestors1996: 2 other ancestors1992: 1 other ancestor2008: 2 other ancestors2005: 1 other ancestor2003: 2 other ancestors2001: 3 other ancestors1998: 1 other ancestor1997: 1 other ancestor1978: 1 other ancestor1999: 1 other ancestor2015: 1 descendant cleared2017: 3 descendants cleared2023: 2 descendants cleared2024: 3 descendants cleared2016: 1 descendant cleared2026: 1 descendant clearedK925812 · Titanium Songer Cable System · Sofamor Danek Mfg., Inc. · 1993K974020 · Spinal Concepts, Inc., Cfix Cable System · Spinal Concepts, Inc. · 1997K060009 · Abbott Spine Universal Clamp System · Abbott Spine, Inc. · 2006K081622 · Universal Clamp Stainless Steel System · Abbott Spine, Inc. · 2008K091190 · Universal Clamp Stainless Steel System, Models SNA027-0-30060, SNA027-0-30063 · Zimmer Spine, Inc. · 2009K110348 · Universal Clamp Spinal Fixation System · Zimmer Spine · 201119801990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 2 other ancestors2 generations back: 4 other ancestors3 generations back: 2 other ancestors4 generations back: 11 other ancestors5 generations back: 3 other ancestors 1 generation forward: 3 descendants2 generations forward: 4 descendants3 generations forward: 2 descendants4 generations forward: 1 descendant5 generations forward: 1 descendant K110348 · Universal Clamp Spinal Fixation System · Zimmer Spine · 2011K091190 · Universal Clamp Stainless Steel System, Models SNA027-0-30060, SNA027-0-30063 · Zimmer Spine, Inc. · 2009K081622 · Universal Clamp Stainless Steel System · Abbott Spine, Inc. · 2008K060009 · Abbott Spine Universal Clamp System · Abbott Spine, Inc. · 2006K974020 · Spinal Concepts, Inc., Cfix Cable System · Spinal Concepts, Inc. · 1997K925812 · Titanium Songer Cable System · Sofamor Danek Mfg., Inc. · 1993−50+5
  1. Root · 6 generations backK925812 Titanium Songer Cable SystemSofamor Danek Mfg., Inc. · 1993
  2. 5 generations backK974020 Spinal Concepts, Inc., Cfix Cable SystemSpinal Concepts, Inc. · 1997
  3. 4 generations backK060009 Abbott Spine Universal Clamp SystemAbbott Spine, Inc. · 2006
  4. 3 generations backK081622 Universal Clamp Stainless Steel SystemAbbott Spine, Inc. · 2008
  5. 2 generations backK091190 Universal Clamp Stainless Steel System, Models SNA027-0-30060…Zimmer Spine, Inc. · 2009
  6. 1 generation backK110348 Universal Clamp Spinal Fixation SystemZimmer Spine · 2011
  7. This deviceK133482 Silc Fixation SystemGlobus Medical, Inc. · 2014
  8. Descendant · cites it directly · 10 of its ownK143350 Nile Alternative FixationK2m, Inc. · 2015
  9. Descendant · 2 generations on · 5 of its ownK161332 NILE Proximal Fixation Spinal SystemK2m, Inc. · 2017
  10. Descendant · 2 generations on · 5 of its ownK160208 NILE Alternative Fixation Spinal SystemK2m, Inc. · 2016
  11. Descendant · 3 generations on · 4 of its ownK222684 XIA® 4.5 Spinal System, XIA® 4.5 Cortical Trajectory, XIA® 3 Spinal…Stryker Spine · 2023
  12. Descendant · 2 generations on · 2 of its ownK163181 TRANSLACE™ Spinal Tethering SystemMedtronic Sofamor Danek USA, Inc. · 2017

Showing 5 of 11 descendants. See all descendants

Descendants cleared per year

2015: 12016: 12017: 32023: 22024: 32026: 1
2015high 3 (2017) · low 0 (2018)2026

Most influential descendants

Showing 5 of 11 · See all
  • K143350Nile Alternative FixationK2m, Inc. · 2015 · cites it directly10descendants
  • K161332NILE Proximal Fixation Spinal SystemK2m, Inc. · 2017 · 2 generations on5descendants
  • K160208NILE Alternative Fixation Spinal SystemK2m, Inc. · 2016 · 2 generations on5descendants
  • K222684XIA® 4.5 Spinal System, XIA® 4.5 Cortical Trajectory, XIA® 3 Spinal System, Serrato®…Stryker Spine · 2023 · 3 generations on4descendants
  • K163181TRANSLACE™ Spinal Tethering SystemMedtronic Sofamor Danek USA, Inc. · 2017 · 2 generations on2descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K925812Titanium Songer Cable SystemSofamor Danek Mfg., Inc.1993—
−5K974020Spinal Concepts, Inc., Cfix Cable SystemSpinal Concepts, Inc.1997—
−4K060009Abbott Spine Universal Clamp SystemAbbott Spine, Inc.2006—
−3K081622Universal Clamp Stainless Steel SystemAbbott Spine, Inc.2008—
−2K091190Universal Clamp Stainless Steel System, Models SNA027-0-30060, SNA027-0-30063Zimmer Spine, Inc.2009—
−1K110348Universal Clamp Spinal Fixation SystemZimmer Spine2011—
0 (this device)K133482Silc Fixation SystemGlobus Medical, Inc.2014—
+1K143350Nile Alternative FixationK2m, Inc.2015—
+2K161332NILE Proximal Fixation Spinal SystemK2m, Inc.2017—
+2K160208NILE Alternative Fixation Spinal SystemK2m, Inc.2016—
+3K222684XIA® 4.5 Spinal System, XIA® 4.5 Cortical Trajectory, XIA® 3 Spinal System…Stryker Spine2023—
+2K163181TRANSLACE™ Spinal Tethering SystemMedtronic Sofamor Danek USA, Inc.2017—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197810
199210
199310
199620
199710
199810
199910
200040
200130
200320
200510
200820
201010
201210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201510
201610
201730
202320
202430
202610
FIG. 1 — Lineage of K133482, 1993–2026Source: 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 OWI? 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 OWI device

  1. #1 K253615 Invictus Bands Systemscore 20.7 · 33 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
*K060009Abbott Spine Universal Clamp System
Summary page 1
…Product Codes OWl Regulatory Class 11,Panel Code 87 Predicate(s): Zimmer Spine Universal Clamp Spinal Fixation System, K060009, K110348 Medicrea LigaPASS, K1 12736 Pioneer Songer Cable System, K922952 Purpose: The p…
Abbott Spine, Inc.2006—
*K110348Universal Clamp Spinal Fixation System
Summary page 1
…Codes OWl Regulatory Class 11,Panel Code 87 Predicate(s): Zimmer Spine Universal Clamp Spinal Fixation System, K060009, K110348 Medicrea LigaPASS, K1 12736 Pioneer Songer Cable System, K922952 Purpose: The purpose of…
Zimmer Spine2011—
*K112736Pass LP Spinal
Summary page 1
…11,Panel Code 87 Predicate(s): Zimmer Spine Universal Clamp Spinal Fixation System, K060009, K110348 Medicrea LigaPASS, K1 12736 Pioneer Songer Cable System, K922952 Purpose: The purpose of this submission is to request clearance of the…
Medicrea International2012—
*K922952Songer Cable System
Summary page 1
…al Clamp Spinal Fixation System, K060009, K110348 Medicrea LigaPASS, K1 12736 Pioneer Songer Cable System, K922952 Purpose: The purpose of this submission is to request clearance of the SILCTM Fixation System. DEVICE DESCRIPTION: The SILCTM Fi…
Pioneer Surgical Technology1993—

Also cleared against K060009: 7 other devices →

What descends from it? (11)

See all 11

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

NumberDeviceApplicantDecidedDescendants
K143350Nile Alternative FixationK2m, Inc.201510
K172417SILC® Fixation SystemGlobus Medical, Inc.20171
K230565HILINE™ Fixation SystemGlobus Medical, Inc.20230

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 6 companies; a new generation was cleared every 2.8 years on median.
  • 1 of the 28 ancestors has a recall of any class.
  • Of its descendants, K143350 (K2m, Inc., 2015) has gone furthest, with 10 descendants of its own.
  • 7 other devices also cite its predicate K060009.

How does its category compare?

All OWI devices

OWI Bone Fixation Cerclage, Sublaminar: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.

FDA decisions per year · OWI

2in 2023

2011: 12013: 22014: 32015: 32016: 52017: 72018: 42019: 32020: 32021: 12022: 12023: 22026 (partial year): 2
2007high 7 (2017) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OWI

60in 2020

2014: 92 days median2015: 93 days median2016: 98 days median2017: 77 days median2018: 156 days median2019: 51 days median2020: 60 days median
2007high 156 (2018) · low 51 (2019)2026

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

Recalls per year · OWI

1in 2020

2020: 1
2007high 1 (2020) · low 0 (2007)2026

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

Adverse event reports per year · OWI

6in 2025

2014: 12015: 12016: 62017: 62018: 22019: 132020: 82021: 52022: 62023: 42024: 32025: 6
2007high 13 (2019) · low 0 (2007)2025

MAUDE reports naming product code OWI, 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
20080—00
20090—00
20100—00
20111—00
20120—00
20132—00
201439201
201539301
201659806
201777706
2018415602
2019351013
202036018
20211—05
20221—06
20232—04
20240—03
20250—06
20262—0—

What is it indicated for?

The SILCTM Fixation System consists of temporary implants for use in orthopedic surgery. The 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, interspinous or facet wiring techniques; * Spinal reconstructive surgery, incorporated into constructs…

Read the full statement (132 words)

The SILCTM Fixation System consists of temporary implants for use in orthopedic surgery. The 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, interspinous or facet wiring techniques;

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

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

The SILCTh Fixation System may also be used in conjunction with other medical implants made of similar metals whenever 'wiring" may help secure the attachment of other implants.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K133482: Silc 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/K133482

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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