510(k) Report

510(k) · Cleared

Cleared

EZ-TRAX Zimmer G7 Acetabular System / Taperloc Complete Hip System Containment Device

K213209510(k) TraditionalCleared Dec 28, 202190-day reviewClass II21 CFR 880.6850

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

K1 Medical, LLC · KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

Cleared on Dec 28, 2021 as substantially equivalent to K211007 (K1 Medical, LLC, 2021) after a 90-day review. Its family tree reaches back 10 generations to 1984.

Decided
Dec 28, 2021
Review
90 days
Class
Class II
Product code
KCT
Recalls
None
Predicates
1

Its longest line of descent runs back 10 generations to K844002 (1984). 16 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 10 generations backK844002 HU-Friedy Ims Cassette SystemHu-Friedy Mfg. Co., Inc. · 1984
  2. 6 generations between
  3. 3 generations backK192487 EZ-TRAX Containment DeviceK1 Medical, LLC · 2019
  4. 2 generations backK202270 EZ-TRAX Stryker Mako Total Knee with Triathlon Containment DeviceK1 Medical, LLC · 2020
  5. 1 generation backK211007 EZ-TRAXTM Persona Knee Containment DeviceK1 Medical, LLC · 2021
  6. This deviceK213209 EZ-TRAX Zimmer G7 Acetabular System / Taperloc Complete Hip System…K1 Medical, LLC · 2021
Show all 10 generations
  1. Root · 10 generations backK844002 HU-Friedy Ims Cassette SystemHu-Friedy Mfg. Co., Inc. · 1984
  2. 9 generations backK980065 C/T Med-Systems Cassette SystemC/T Med System, Ltd. · 1998
  3. 8 generations backK990761 Tuttnauer Mini Container Cassette, Tuttnauer Standard Case CassetteTuttnauer U.S.A Co, Ltd. · 1999
  4. 7 generations backK012105 Polyvac Surgical Instrument Delivery SystemSymmetry Medical, Inc. · 2002
  5. 6 generations backK040223 Polyvac Instrument Delivery SystemSymmetry Medical USA, Inc. · 2004
  6. 5 generations backK120947 THS Instrument TrayHologic, Inc. · 2012
  7. 4 generations backK152241 Medtronic Transportation/Sterilization CassettesMedtronic Sofamor Danek USA, Inc. · 2016
  8. 3 generations backK192487 EZ-TRAX Containment DeviceK1 Medical, LLC · 2019
  9. 2 generations backK202270 EZ-TRAX Stryker Mako Total Knee with Triathlon Containment DeviceK1 Medical, LLC · 2020
  10. 1 generation backK211007 EZ-TRAXTM Persona Knee Containment DeviceK1 Medical, LLC · 2021
  11. This deviceK213209 EZ-TRAX Zimmer G7 Acetabular System / Taperloc Complete Hip System…K1 Medical, LLC · 2021
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−10K844002HU-Friedy Ims Cassette SystemHu-Friedy Mfg. Co., Inc.1984—
−9K980065C/T Med-Systems Cassette SystemC/T Med System, Ltd.1998—
−8K990761Tuttnauer Mini Container Cassette, Tuttnauer Standard Case CassetteTuttnauer U.S.A Co, Ltd.1999—
−7K012105Polyvac Surgical Instrument Delivery SystemSymmetry Medical, Inc.2002—
−6K040223Polyvac Instrument Delivery SystemSymmetry Medical USA, Inc.2004—
−5K120947THS Instrument TrayHologic, Inc.2012—
−4K152241Medtronic Transportation/Sterilization CassettesMedtronic Sofamor Danek USA, Inc.2016—
−3K192487EZ-TRAX Containment DeviceK1 Medical, LLC2019—
−2K202270EZ-TRAX Stryker Mako Total Knee with Triathlon Containment DeviceK1 Medical, LLC2020—
−1K211007EZ-TRAXTM Persona Knee Containment DeviceK1 Medical, LLC2021—
0 (this device)K213209EZ-TRAX Zimmer G7 Acetabular System / Taperloc Complete Hip System Containment…K1 Medical, LLC2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
199710
200110
200210
200410
201310
FIG. 1 — Lineage of K213209, 1984–2021Source: 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 KCT? 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 KCT device

  1. #1 K214041 Aesculap AICON Containerscore 18.1 · 6 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? (1)

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
*K211007EZ-TRAXTM Persona Knee Containment Device
Summary page 5
…terilization Wrap Regulatory Class: Class II, 21 CFR 880.6850 Product Code: KCT II. PREDICATE DEVICE: EZ-TRAX™ Persona Knee Containment Device K211007 Ill.DEVICE DESCRIPTION The EZ-TRAX™ Zimmer G7 Acetabular System/ Taperloc Complete Hip System Containment Device is…
K1 Medical, LLC2021—

What descends from it?

No later submission names this one as a predicate yet.

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 37 years and passes through 8 companies; a new generation was cleared every 3.1 years on median.
  • None of the 16 ancestors has a recall.

How does its category compare?

All KCT devices

KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.

FDA decisions per year · KCT

11in 2025

2007: 32008: 62009: 62010: 122011: 62012: 102013: 82014: 112015: 152016: 122017: 102018: 152019: 182020: 142021: 182022: 112023: 102024: 82025: 112026 (partial year): 9
2007high 18 (2019) · low 3 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KCT

205in 2025

2007: 199 days median2008: 182 days median2009: 89 days median2010: 202 days median2011: 117 days median2012: 236 days median2013: 131 days median2014: 169 days median2015: 151 days median2016: 182 days median2017: 211 days median2018: 192 days median2019: 187 days median2020: 134 days median2021: 185 days median2022: 137 days median2023: 94 days median2024: 106 days median2025: 205 days median2026 (partial year): 122 days median
2007high 236 (2012) · low 89 (2009)2026

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

Recalls per year · KCT

17in 2022

2010: 12011: 22013: 12014: 12016: 32017: 12021: 12022: 17
2007high 17 (2022) · low 0 (2007)2026

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

Adverse event reports per year · KCT

50in 2025

2007: 22008: 82009: 52010: 32011: 32012: 22013: 62014: 52015: 62016: 162017: 32018: 222019: 152020: 662021: 262022: 82023: 302024: 182025: 50
2007high 66 (2020) · low 2 (2007)2025

MAUDE reports naming product code KCT, 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
2007319902
2008618208
200968905
20101220213
2011611723
20121023602
2013813116
20141116915
20151515106
201612182316
20171021113
201815192022
201918187015
202014134066
202118185126
202211137178
20231094030
20248106018
202511205050
202691220—

What is it indicated for?

The EZ-TRAX ™ Zimmer G7 Acetabular System I Taperloc Complete Hip System Containment Device is intended for use as an accessory in healthcare facilities to organize, enclose, reprocess, transport, and store Zimmer G7 Acetabular System I Taperloc Complete Hip System devices between surgical uses. The EZ-TRAX ™ Zimmer G7 Acetabular System I Taperloc Complete Hip System Containment Device is not intended on its own to maintain sterility; it is intended to be used in conjunction with a legally marketed, validated, FDA-cleared sterile barrier system.

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

Cite this page

510(k) Report. “K213209: EZ-TRAX Zimmer G7 Acetabular System / Taperloc Complete Hip System Containment Device.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K213209

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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