510(k) Report

510(k) · Cleared

Cleared

Monster BITE Screw System

K153378510(k) SpecialCleared Dec 21, 201528-day reviewClass II21 CFR 888.3040

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

Paragon 28 · HWC Screw, Fixation, Bone

Cleared on Dec 21, 2015 as substantially equivalent to K151418 (Paragon 28, 2015) after a 28-day review. Its family tree reaches back 12 generations to 1996. 22 later devices descend from it.

Decided
Dec 21, 2015
Review
28 days
Class
Class II
Product code
HWC
Recalls
None
Predicates
1

Its longest line of descent runs back 12 generations to K962616 (1996). 84 ancestors in all, the oldest K792022 (1979). 22 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2011: 1 other ancestor2010: 1 other ancestor2009: 2 other ancestors2006: 8 other ancestors2005: 5 other ancestors2002: 4 other ancestors2001: 7 other ancestors1999: 5 other ancestors1998: 4 other ancestors1996: 6 other ancestors1993: 2 other ancestors2008: 2 other ancestors2007: 1 other ancestor2003: 2 other ancestors2000: 7 other ancestors1995: 3 other ancestors1990: 1 other ancestor1989: 2 other ancestors1987: 1 other ancestor1979: 1 other ancestor2004: 4 other ancestors1994: 2 other ancestors1991: 1 other ancestor2019: 1 descendant cleared2020: 3 descendants cleared2022: 3 descendants cleared2021: 1 descendant cleared2023: 6 descendants cleared2024: 2 descendants cleared2025: 2 descendants cleared2026: 4 descendants clearedReference device: K124027 · Monster Screw System · Apogee Orthosolutions · 2013Reference device: K090675 · Smith & Nephew, Inc. VLP Foot Plating, Screw System and Accessories · Smith & Nephew, Inc. · 2009Reference device: K924018 · M3 Lag Screw Fixation System · Osteomed Corp. · 1993K962616 · Synthes Dorsal Distal Radius Plate (DDRP) System · Synthes (Usa) · 1996K982732 · Synthes (Usa) Distal Radius Plate System (DRPS) · Synthes · 1998×3: 3 generations cleared close together, K023007 (2002), K030198 (2003), K032705 (2003) ×2: 2 generations cleared close together, K050932 (2005), K051735 (2005) K071563 · Peri-Loc Periarticular Locked Plating System · Smith & Nephew, Inc. · 2007K090675 · Smith & Nephew, Inc. VLP Foot Plating, Screw System and Accessories · Smith & Nephew, Inc. · 2009K111994 · Smith & Nephew Cannulated Screws and Washers · Smith & Nephew, Inc. · 2011K124027 · Monster Screw System · Apogee Orthosolutions · 2013K151418 · Monster Screw System · Paragon 28 · 201519801990200020102020
Other ancestors, by generationDescendants, by generation 3 generations back: 16 other ancestors4 generations back: 17 other ancestors5 generations back: 15 other ancestors6 generations back: 11 other ancestors7 generations back: 6 other ancestors8 generations back: 2 other ancestors9 generations back: 3 other ancestors10 generations back: 1 other ancestor11 generations back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 6 descendants3 generations forward: 9 descendants4 generations forward: 5 descendants5 generations forward: 1 descendant K151418 · Monster Screw System · Paragon 28 · 2015K124027 · Monster Screw System · Apogee Orthosolutions · 2013K111994 · Smith & Nephew Cannulated Screws and Washers · Smith & Nephew, Inc. · 2011K090675 · Smith & Nephew, Inc. VLP Foot Plating, Screw System and Accessories · Smith & Nephew, Inc. · 2009K071563 · Peri-Loc Periarticular Locked Plating System · Smith & Nephew, Inc. · 2007K051735 · Peri-Loc Locking Bone Plates and Locking Bone Screws for the Upper Extremity · Smith & Nephew, Inc. · 2005K050932 · Distal Volar Radius Anatomical Plate System · Hand Innovations, Inc. · 2005 · recalledK032705 · Distal Radius Fracture Repair System · Hand Innovations, Inc. · 2003K030198 · Hand Innovations, Inc. Distal Radius Fracture Repair System · Hand Innovations, Inc. · 2003K023007 · Distal Radius Fracture Repair System · Hand Innovations, Inc. · 2002K982732 · Synthes (Usa) Distal Radius Plate System (DRPS) · Synthes · 1998K962616 · Synthes Dorsal Distal Radius Plate (DDRP) System · Synthes (Usa) · 1996−10−50+5
  1. Root · 12 generations backK962616 Synthes Dorsal Distal Radius Plate (DDRP) SystemSynthes (Usa) · 1996
  2. 8 generations between
  3. 3 generations backK111994 Smith & Nephew Cannulated Screws and WashersSmith & Nephew, Inc. · 2011
  4. 2 generations backK124027 Monster Screw SystemApogee Orthosolutions · 2013
  5. 1 generation backK151418 Monster Screw SystemParagon 28 · 2015
  6. This deviceK153378 Monster BITE Screw SystemParagon 28 · 2015
  7. Descendant · cites it directly · 21 of its ownK190586 Monster® Screw SystemParagon 28, Inc. · 2019
  8. Descendant · 2 generations on · 9 of its ownK200398 AxSOS 3 AF System and AxSOS 3 Ti SystemStryker GmbH · 2020
  9. Descendant · 3 generations on · 8 of its ownK222381 PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti…Stryker GmbH · 2023
  10. Descendant · 2 generations on · 6 of its ownK203011 Monster Screw SystemParagon 28, Inc. · 2020
  11. Descendant · 3 generations on · 4 of its ownK231262 Pangea Femur Plating System, Pangea Fibula Plating System, Pangea…Stryker GmbH · 2023
Show all 12 generations
  1. Root · 12 generations backK962616 Synthes Dorsal Distal Radius Plate (DDRP) SystemSynthes (Usa) · 1996
  2. 11 generations backK982732 Synthes (Usa) Distal Radius Plate System (DRPS)Synthes · 1998
  3. 10 generations backK023007 Distal Radius Fracture Repair SystemHand Innovations, Inc. · 2002
  4. 9 generations backK030198 Hand Innovations, Inc. Distal Radius Fracture Repair SystemHand Innovations, Inc. · 2003
  5. 8 generations backK032705 Distal Radius Fracture Repair SystemHand Innovations, Inc. · 2003
  6. 7 generations backK050932 Distal Volar Radius Anatomical Plate SystemHand Innovations, Inc. · 2005 · Recalled
  7. 6 generations backK051735 Peri-Loc Locking Bone Plates and Locking Bone Screws for the Upper…Smith & Nephew, Inc. · 2005
  8. 5 generations backK071563 Peri-Loc Periarticular Locked Plating SystemSmith & Nephew, Inc. · 2007
  9. 4 generations backK090675 Smith & Nephew, Inc. VLP Foot Plating, Screw System and AccessoriesSmith & Nephew, Inc. · 2009
  10. 3 generations backK111994 Smith & Nephew Cannulated Screws and WashersSmith & Nephew, Inc. · 2011
  11. 2 generations backK124027 Monster Screw SystemApogee Orthosolutions · 2013
  12. 1 generation backK151418 Monster Screw SystemParagon 28 · 2015
  13. This deviceK153378 Monster BITE Screw SystemParagon 28 · 2015

Showing 5 of 22 descendants. See all descendants

Descendants cleared per year

2019: 12020: 32021: 12022: 32023: 62024: 22025: 22026: 4
2019high 6 (2023) · low 1 (2019)2026

Most influential descendants

Showing 5 of 22 · See all
  • K190586Monster® Screw SystemParagon 28, Inc. · 2019 · cites it directly21descendants
  • K200398AxSOS 3 AF System and AxSOS 3 Ti SystemStryker GmbH · 2020 · 2 generations on9descendants
  • K222381PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating SystemStryker GmbH · 2023 · 3 generations on8descendants
  • K203011Monster Screw SystemParagon 28, Inc. · 2020 · 2 generations on6descendants
  • K231262Pangea Femur Plating System, Pangea Fibula Plating System, Pangea Tibia Plating System…Stryker GmbH · 2023 · 3 generations on4descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−12K962616Synthes Dorsal Distal Radius Plate (DDRP) SystemSynthes (Usa)1996—
−11K982732Synthes (Usa) Distal Radius Plate System (DRPS)Synthes1998—
−10K023007Distal Radius Fracture Repair SystemHand Innovations, Inc.2002—
−9K030198Hand Innovations, Inc. Distal Radius Fracture Repair SystemHand Innovations, Inc.2003—
−8K032705Distal Radius Fracture Repair SystemHand Innovations, Inc.2003—
−7K050932Distal Volar Radius Anatomical Plate SystemHand Innovations, Inc.20051
−6K051735Peri-Loc Locking Bone Plates and Locking Bone Screws for the Upper ExtremitySmith & Nephew, Inc.2005—
−5K071563Peri-Loc Periarticular Locked Plating SystemSmith & Nephew, Inc.2007—
−4K090675Smith & Nephew, Inc. VLP Foot Plating, Screw System and AccessoriesSmith & Nephew, Inc.2009—
−3K111994Smith & Nephew Cannulated Screws and WashersSmith & Nephew, Inc.2011—
−2K124027Monster Screw SystemApogee Orthosolutions2013—
−1K151418Monster Screw SystemParagon 282015—
0 (this device)K153378Monster BITE Screw SystemParagon 282015—
+1K190586Monster® Screw SystemParagon 28, Inc.2019—
+2K200398AxSOS 3 AF System and AxSOS 3 Ti SystemStryker GmbH2020—
+3K222381PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker…Stryker GmbH2023—
+2K203011Monster Screw SystemParagon 28, Inc.2020—
+3K231262Pangea Femur Plating System, Pangea Fibula Plating System, Pangea Tibia…Stryker GmbH2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197910
198710
198920
199010
199110
199320
199420
199530
199660
199840
199950
200070
200170
200240
200320
200440
200550
200680
200710
200820
200920
201010
201110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201910
202030
202110
202230
202360
202420
202520
202640
FIG. 1 — Lineage of K153378, 1996–2026Source: 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 HWC? 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 HWC device

  1. #1 K203011 Monster Screw Systemscore 22.2 · 14 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
*K151418Monster Screw System
Summary page 4
…BITE Screw System™ implants are manufactured from medical grade titanium alloy (per ASTM F136). Predicate Devices: Primary: Paragon 28 (K151418) Reference Devices: Paragon 28 (K124027) Smith & Nephew (K090675) Oste…
Paragon 282015—
†K124027Monster Screw SystemApogee Orthosolutions2013—
†K090675Smith & Nephew, Inc. VLP Foot Plating, Screw System and AccessoriesSmith & Nephew, Inc.2009—
†K924018M3 Lag Screw Fixation SystemOsteomed Corp.1993—

Also cleared against K151418: 4 other devices →

What descends from it? (22)

See all 22

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

NumberDeviceApplicantDecidedDescendants
K190586Monster® Screw SystemParagon 28, Inc.201921

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 19 years and passes through 6 companies; a new generation was cleared every 1.8 years on median.
  • 20 of the 84 ancestors have a recall of any class.
  • Of its descendants, K190586 (Paragon 28, Inc., 2019) has gone furthest, with 21 descendants of its own.
  • 4 other devices also cite its predicate K151418.

How does its category compare?

All HWC devices

HWC Screw, Fixation, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.

FDA decisions per year · HWC

15in 2025

2007: 352008: 332009: 272010: 232011: 352012: 202013: 252014: 312015: 412016: 262017: 402018: 202019: 302020: 282021: 262022: 262023: 242024: 172025: 152026 (partial year): 21
2007high 41 (2015) · low 15 (2025)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HWC

111in 2025

2007: 77 days median2008: 76 days median2009: 113 days median2010: 110 days median2011: 88 days median2012: 99 days median2013: 90 days median2014: 88 days median2015: 85 days median2016: 131 days median2017: 127 days median2018: 106 days median2019: 108 days median2020: 75 days median2021: 84 days median2022: 167 days median2023: 104 days median2024: 90 days median2025: 111 days median2026 (partial year): 125 days median
2007high 167 (2022) · low 75 (2020)2026

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

Recalls per year · HWC

1in 2025

2007: 252008: 332009: 292010: 72011: 122012: 302013: 142014: 22015: 52016: 42017: 42018: 12019: 52020: 42021: 22022: 132025: 12026 (partial year): 2
2007high 33 (2008) · low 0 (2023)2026

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

Adverse event reports per year · HWC

2,893in 2025

2007: 6692008: 6602009: 6512010: 7652011: 1,1042012: 3,3392013: 3,8502014: 2,5492015: 2,7112016: 2,2852017: 2,5612018: 3,6622019: 5,4632020: 4,8202021: 4,4462022: 3,9342023: 3,7182024: 3,5752025: 2,893
2007high 5,463 (2019) · low 651 (2009)2025

MAUDE reports naming product code HWC, 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
2007357725669
2008337633660
20092711329651
2010231107765
20113588121,104
20122099303,339
20132590143,850
2014318822,549
2015418552,711
20162613142,285
20174012742,561
20182010613,662
20193010855,463
2020287544,820
2021268424,446
202226167133,934
20232410403,718
2024179003,575
20251511112,893
2026211252—

What is it indicated for?

The Monster BITE Screw System™ is indicated for use in bone reconstruction, osteotomy, arthrodesis, joint fusion, ligament fixation, fracture repair and fracture fixation, appropriate for the size of the device

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K153378: Monster BITE Screw System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K153378

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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