510(k) Report

510(k) · Cleared

Cleared

OsteoMed QuickFix Hybrid MMF Sterilization Tray

K173391510(k) TraditionalCleared May 10, 2018192-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

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

Cleared on May 10, 2018 as substantially equivalent to K143579 (Nu Vasive, Incorporated, 2015) after a 192-day review. Its family tree reaches back 8 generations to 1984. 2 later devices descend from it.

Decided
May 10, 2018
Review
192 days
Class
Class II
Product code
KCT
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K844002 (1984). 11 ancestors in all. 2 later devices descend from it, 2 citing it directly.

  1. Root · 8 generations backK844002 HU-Friedy Ims Cassette SystemHu-Friedy Mfg. Co., Inc. · 1984
  2. 7 generations backK980065 C/T Med-Systems Cassette SystemC/T Med System, Ltd. · 1998
  3. 6 generations backK990761 Tuttnauer Mini Container Cassette, Tuttnauer Standard Case CassetteTuttnauer U.S.A Co, Ltd. · 1999
  4. 5 generations backK012105 Polyvac Surgical Instrument Delivery SystemSymmetry Medical, Inc. · 2002
  5. 4 generations backK073551 Smith & Nephew Instrument TraysSmith & Nephew Inc., Endoscopy Div. · 2008
  6. 3 generations backK090562 Smith & Nephew Instrument TraysSmith & Nephew, Inc. · 2009
  7. 2 generations backK102103 Skeletal Dynamics Sterilization TraysSkeletal Dynamics, LLC · 2010
  8. 1 generation backK143579 NuVasive Sterilization TraysNu Vasive, Incorporated · 2015
  9. This deviceK173391 OsteoMed QuickFix Hybrid MMF Sterilization TrayOsteomed, LLC · 2018
  10. Descendant · cites it directly · 0 of its ownK212068 Biotech Dental KitsBiotech Dental, Sas · 2021
  11. Descendant · cites it directly · 0 of its ownK202105 OsteoMed ExtremiFix Mini & Small System TrayOsteomed, LLC · 2020

Most influential descendants

Showing 2 of 2 · See all
  • K212068Biotech Dental KitsBiotech Dental, Sas · 2021 · cites it directly0descendants
  • K202105OsteoMed ExtremiFix Mini & Small System TrayOsteomed, LLC · 2020 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K844002HU-Friedy Ims Cassette SystemHu-Friedy Mfg. Co., Inc.1984—
−7K980065C/T Med-Systems Cassette SystemC/T Med System, Ltd.1998—
−6K990761Tuttnauer Mini Container Cassette, Tuttnauer Standard Case CassetteTuttnauer U.S.A Co, Ltd.1999—
−5K012105Polyvac Surgical Instrument Delivery SystemSymmetry Medical, Inc.2002—
−4K073551Smith & Nephew Instrument TraysSmith & Nephew Inc., Endoscopy Div.2008—
−3K090562Smith & Nephew Instrument TraysSmith & Nephew, Inc.2009—
−2K102103Skeletal Dynamics Sterilization TraysSkeletal Dynamics, LLC2010—
−1K143579NuVasive Sterilization TraysNu Vasive, Incorporated2015—
0 (this device)K173391OsteoMed QuickFix Hybrid MMF Sterilization TrayOsteomed, LLC2018—
+1K212068Biotech Dental KitsBiotech Dental, Sas2021—
+1K202105OsteoMed ExtremiFix Mini & Small System TrayOsteomed, LLC2020—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
199710
200110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
202110
FIG. 1 — Lineage of K173391, 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
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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
*K143579NuVasive Sterilization Trays
Summary page 4
…880.6850 Regulatory Class: II Product Code: KCT III. PREDICATE DEVICE Primary Predicate: NuVasive® Sterilization Trays (K143579) IV. DEVICE DESCRIPTION The OsteoMed MMF Sterilization Tray is composed from a material commonly used (anodiz…
Nu Vasive, Incorporated2015—

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K212068Biotech Dental KitsBiotech Dental, Sas20210
K202105OsteoMed ExtremiFix Mini & Small System TrayOsteomed, LLC20200

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 34 years and passes through 9 companies; a new generation was cleared every 3.1 years on median.
  • None of the 11 ancestors has a recall.
  • Of its descendants, K212068 (Biotech Dental, Sas, 2021) has gone furthest, with 0 descendants of its own.

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. 2018, 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 OsteoMed MMF Sterilization Tray is intended to contain MMF implants and surgical instruments for sterilization, storage and handling. The OsteoMed MMF Sterilization Tray is suitable for dynamic air removal (pre-vacuum) steam sterilization methods. The tray is not intended to maintain sterility; it is intended to be used in conjunction with a validated, FDA-cleared sterilization wrap in order to maintain sterility of the enclosed devices. The…

Read the full statement (130 words)

The OsteoMed MMF Sterilization Tray is intended to contain MMF implants and surgical instruments for sterilization, storage and handling. The OsteoMed MMF Sterilization Tray is suitable for dynamic air removal (pre-vacuum) steam sterilization methods. The tray is not intended to maintain sterility; it is intended to be used in conjunction with a validated, FDA-cleared sterilization wrap in order to maintain sterility of the enclosed devices. The sterilization tray may also be used in conjunction with a legally marketed rigid container.

Sterilization validation was performed on MMF implants and accessories such as surgical instrumentation. Do not exceed a maximum load of 2.3 Ibs. in the sterilization tray.

Validated sterilization parameters for OsteoMed MMF Sterilization Tray:

Method: Steam Cycle

Pre-Vacuum Temperature: 270°F (132°C)

Exposure Time: 4 minutes

Minimum Dry Time: 30 minutes

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. “K173391: OsteoMed QuickFix Hybrid MMF Sterilization Tray.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K173391

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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