510(k) Report

510(k) · Cleared

Cleared

Zimmer Natural Nail System Cephalomedullary Nails

K192312510(k) SpecialCleared Oct 11, 201946-day reviewClass II21 CFR 888.3020

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

Zimmer GmbH · HSB Rod, Fixation, Intramedullary And Accessories

Cleared on Oct 11, 2019 as substantially equivalent to K091566 (Zimmer GmbH, 2009) and 1 other predicate after a 46-day review. Its family tree reaches back 7 generations to 1997. 4 later devices descend from it.

Decided
Oct 11, 2019
Review
46 days
Class
Class II
Product code
HSB
Recalls
None
Predicates
2

Its longest line of descent runs back 7 generations to K970097 (1997). 20 ancestors in all, the oldest K871539 (1987). 4 later devices descend from it, 1 citing it directly.

  1. Root · 7 generations backK970097 Proximal Femoral Nail (PFN) SystemSynthes (Usa) · 1997
  2. 6 generations backK973240 Synthes Proximal Femoral Nail (PFN) System ModificationSynthes (Usa) · 1997
  3. 5 generations backK013563 Long Trochanteric Nail SystemDePuy Orthopaedics, Inc. · 2001 · Recalled
  4. 4 generations backK033329 Depuy Ace Universal and Troch Entry Femoral Nail SystemsDepuy, Inc. · 2003
  5. 3 generations backK083497 Zimmer Natural Nail System Piriformis Fossa and Greater Trochanter…Zimmer, Inc. · 2009 · Recalled
  6. 2 generations backK091566 Zimmer Natural Nail System Cephalomedullary NailsZimmer GmbH · 2009 · Recalled
  7. 1 generation backK120715 Zimmer Natural Nail System Cephalomedullary Femoral Nail - Asia ShortZimmer GmbH · 2012
  8. This deviceK192312 Zimmer Natural Nail System Cephalomedullary NailsZimmer GmbH · 2019
  9. Descendant · cites it directly · 3 of its ownK213328 Gamma4 System, Gamma3 System, IMN Screws System, T2 Tibial Nailing…Stryker GmbH · 2022 · Recalled
  10. Descendant · 2 generations on · 0 of its ownK251400 T2 Alpha Humerus Nailing System; IMN Screws System; T2 Nailing SystemStryker GmbH · 2025
  11. Descendant · 2 generations on · 0 of its ownK230512 Gamma4 SystemStryker GmbH · 2023
  12. Descendant · 2 generations on · 0 of its ownK222309 Gamma4 SystemStryker GmbH · 2022

Most influential descendants

Showing 4 of 4 · See all
  • K213328Gamma4 System, Gamma3 System, IMN Screws System, T2 Tibial Nailing SystemStryker GmbH · 2022 · cites it directly3descendants
  • K251400T2 Alpha Humerus Nailing System; IMN Screws System; T2 Nailing SystemStryker GmbH · 2025 · 2 generations on0descendants
  • K230512Gamma4 SystemStryker GmbH · 2023 · 2 generations on0descendants
  • K222309Gamma4 SystemStryker GmbH · 2022 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K970097Proximal Femoral Nail (PFN) SystemSynthes (Usa)1997—
−6K973240Synthes Proximal Femoral Nail (PFN) System ModificationSynthes (Usa)1997—
−5K013563Long Trochanteric Nail SystemDePuy Orthopaedics, Inc.200154
−4K033329Depuy Ace Universal and Troch Entry Femoral Nail SystemsDepuy, Inc.2003—
−3K083497Zimmer Natural Nail System Piriformis Fossa and Greater Trochanter Antegrade…Zimmer, Inc.200916
−2K091566Zimmer Natural Nail System Cephalomedullary NailsZimmer GmbH20095
−1K120715Zimmer Natural Nail System Cephalomedullary Femoral Nail - Asia ShortZimmer GmbH2012—
0 (this device)K192312Zimmer Natural Nail System Cephalomedullary NailsZimmer GmbH2019—
+1K213328Gamma4 System, Gamma3 System, IMN Screws System, T2 Tibial Nailing SystemStryker GmbH20221
+2K251400T2 Alpha Humerus Nailing System; IMN Screws System; T2 Nailing SystemStryker GmbH2025—
+2K230512Gamma4 SystemStryker GmbH2023—
+2K222309Gamma4 SystemStryker GmbH2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198710
199620
199710
199820
200120
200220
200310
200410
200510

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202220
202310
202510
FIG. 1 — Lineage of K192312, 1997–2025Source: 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 HSB? 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 HSB device

  1. #1 K200869 Gamma3 Systemscore 19.8 · 8 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? (2)

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
*K091566Zimmer Natural Nail System Cephalomedullary Nails
Summary page 4
…llary fixation rod Predicate Device: Zimmer Natural Nail System Cephalomedullary Nails, manufactured by Zimmer GmbH, K091566, cleared October 2009 and its line extension Zimmer Natural Nail System Cephalomedullary Femor…
Zimmer GmbH20095
*K120715Zimmer Natural Nail System Cephalomedullary Femoral Nail - Asia Short
Summary page 4
…extension Zimmer Natural Nail System Cephalomedullary Femoral Nails – Asia Short, manufactured by Zimmer GmbH, K120715, cleared October 2012 Device Description: The Zimmer® Natural Nail® System Cep…
Zimmer GmbH2012—

Also cleared against K091566: 5 other devices →

What descends from it? (4)

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

NumberDeviceApplicantDecidedDescendants
K213328Gamma4 System, Gamma3 System, IMN Screws System, T2 Tibial Nailing SystemStryker GmbH20223

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 22 years and passes through 5 companies; a new generation was cleared every 2.8 years on median.
  • 12 of the 20 ancestors have a recall of any class.
  • Of its descendants, K213328 (Stryker GmbH, 2022) has gone furthest, with 3 descendants of its own.
  • 5 other devices also cite its predicate K091566.

How does its category compare?

All HSB devices

HSB Rod, Fixation, Intramedullary And Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.

FDA decisions per year · HSB

15in 2025

2007: 82008: 112009: 182010: 142011: 162012: 172013: 182014: 192015: 222016: 82017: 232018: 172019: 132020: 172021: 102022: 122023: 112024: 132025: 152026 (partial year): 18
2007high 23 (2017) · low 8 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HSB

106in 2025

2007: 68 days median2008: 57 days median2009: 86 days median2010: 117 days median2011: 78 days median2012: 112 days median2013: 105 days median2014: 147 days median2015: 111 days median2016: 124 days median2017: 119 days median2018: 134 days median2019: 132 days median2020: 112 days median2021: 94 days median2022: 172 days median2023: 162 days median2024: 195 days median2025: 106 days median2026 (partial year): 151 days median
2007high 195 (2024) · low 57 (2008)2026

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

Recalls per year · HSB

18in 2025

2008: 92009: 812010: 182011: 22012: 72013: 142014: 32015: 32016: 62017: 662018: 562019: 62020: 62021: 22022: 12023: 12024: 12025: 182026 (partial year): 1
2007high 81 (2009) · low 0 (2007)2026

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

Adverse event reports per year · HSB

2,911in 2025

2007: 1622008: 1842009: 3342010: 4542011: 6622012: 1,0792013: 1,7732014: 1,4742015: 1,6712016: 1,9202017: 1,4472018: 3,5262019: 2,5172020: 3,2992021: 4,1112022: 2,7332023: 2,2192024: 2,8692025: 2,911
2007high 4,111 (2021) · low 162 (2007)2025

MAUDE reports naming product code HSB, 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
20078680162
200811579184
2009188681334
20101411718454
201116782662
20121711271,079
201318105141,773
20141914731,474
20152211131,671
2016812461,920
201723119661,447
201817134563,526
20191313262,517
20201711263,299
2021109424,111
20221217212,733
20231116212,219
20241319512,869
202515106182,911
2026181511—

What is it indicated for?

The Zimmer Natural Nail System is intended for temporary fracture fixation and stabilization of the bone.

Indications for the Cephalomedullary nails include:

• Compound and simple shaft fractures

• Proximal, metaphyseal and distal shaft fractures

• Segmental fractures

• Comminuted fractures

• Fractures involving osteopenic and osteoporotic bone

• Pathological fractures

• Fractures with bone loss

• Pseudoarthrosis, non-union, mal-union and delayed union

• Periprosthetic fractures

• Surgically created defects such as osteotomies

• Intertrochanteric and subtrochanteric fractures

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K192312: Zimmer Natural Nail System Cephalomedullary Nails.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K192312

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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