510(k) Report

510(k) · Cleared

Cleared

Baby Gorilla®/Gorilla® Plating System

K222194510(k) SpecialCleared Aug 19, 202228-day reviewClass II21 CFR 888.3030

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

Paragon 28, Inc. · HRS Plate, Fixation, Bone

Cleared on Aug 19, 2022 as substantially equivalent to K221465 (Paragon 28, Inc., 2022) after a 28-day review. Its family tree reaches back 3 generations to 2019. 5 later devices descend from it.

Decided
Aug 19, 2022
Review
28 days
Class
Class II
Product code
HRS
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K190365 (2019). 5 later devices descend from it, 3 citing it directly.

Descendants, by year cleared 2023: 2 descendants cleared2024: 3 descendants clearedK190365 · Baby Gorilla/Gorilla Plating System · Paragon 28, Inc. · 2019K203511 · Baby Gorilla/Gorilla Plating System · Paragon 28, Inc. · 2020K221465 · Baby Gorilla/Gorilla Plating System · Paragon 28, Inc. · 2022201620182020202220242026
Descendants, by generation 1 generation forward: 3 descendants2 generations forward: 2 descendants K221465 · Baby Gorilla/Gorilla Plating System · Paragon 28, Inc. · 2022K203511 · Baby Gorilla/Gorilla Plating System · Paragon 28, Inc. · 2020K190365 · Baby Gorilla/Gorilla Plating System · Paragon 28, Inc. · 20190
  1. Root · 3 generations backK190365 Baby Gorilla/Gorilla Plating SystemParagon 28, Inc. · 2019
  2. 2 generations backK203511 Baby Gorilla/Gorilla Plating SystemParagon 28, Inc. · 2020
  3. 1 generation backK221465 Baby Gorilla/Gorilla Plating SystemParagon 28, Inc. · 2022
  4. This deviceK222194 Baby Gorilla®/Gorilla® Plating SystemParagon 28, Inc. · 2022
  5. Descendant · cites it directly · 1 of its ownK231231 MR Safety and Compatibility Testing and Labeling for Paragon 28…Paragon 28, Inc. · 2023
  6. Descendant · cites it directly · 1 of its ownK221150 Advanced Bone PlateDouble Medical Technology, Inc. · 2023
  7. Descendant · 2 generations on · 0 of its ownK242348 Locking Screw,CoCrMoDouble Medical Technology, Inc. · 2024
  8. Descendant · 2 generations on · 0 of its ownK241262 Baby Gorilla/Gorilla Plating System; Monster Screw SystemParagon 28, Inc. · 2024
  9. Descendant · cites it directly · 0 of its ownK233863 TriMed ASET Foot Plating System (1ST MTP 9-hole Long Plate), TriMed…TriMed, Inc. · 2024

Most influential descendants

Showing 5 of 5 · See all
  • K231231MR Safety and Compatibility Testing and Labeling for Paragon 28 Orthopedic Fixation…Paragon 28, Inc. · 2023 · cites it directly1descendant
  • K221150Advanced Bone PlateDouble Medical Technology, Inc. · 2023 · cites it directly1descendant
  • K242348Locking Screw,CoCrMoDouble Medical Technology, Inc. · 2024 · 2 generations on0descendants
  • K241262Baby Gorilla/Gorilla Plating System; Monster Screw SystemParagon 28, Inc. · 2024 · 2 generations on0descendants
  • K233863TriMed ASET Foot Plating System (1ST MTP 9-hole Long Plate), TriMed ASET Foot Plating…TriMed, Inc. · 2024 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K190365Baby Gorilla/Gorilla Plating SystemParagon 28, Inc.2019—
−2K203511Baby Gorilla/Gorilla Plating SystemParagon 28, Inc.2020—
−1K221465Baby Gorilla/Gorilla Plating SystemParagon 28, Inc.2022—
0 (this device)K222194Baby Gorilla®/Gorilla® Plating SystemParagon 28, Inc.2022—
+1K231231MR Safety and Compatibility Testing and Labeling for Paragon 28 Orthopedic…Paragon 28, Inc.2023—
+1K221150Advanced Bone PlateDouble Medical Technology, Inc.2023—
+2K242348Locking Screw,CoCrMoDouble Medical Technology, Inc.2024—
+2K241262Baby Gorilla/Gorilla Plating System; Monster Screw SystemParagon 28, Inc.2024—
+1K233863TriMed ASET Foot Plating System (1ST MTP 9-hole Long Plate), TriMed ASET Foot…TriMed, Inc.2024—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202320
202430
FIG. 1 — Lineage of K222194, 2019–2024Source: 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 HRS? 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 HRS device

  1. #1 K222465 Tyber Medical Anatomical Plating Systemscore 27.5 · 16 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
*K221465Baby Gorilla/Gorilla Plating System
Summary page 5
…HRS, HWC, HTN Common Name: Bone Plate, Bone Screw, Bone Washer Predicate Device: Baby Gorilla®/Gorilla® Plating System (K221465) Indications for Use: The Baby Gorilla®/Gorilla® Bone Plates and Bone Screws of the Baby Gorilla®/Gorilla® Plating System are in…
Paragon 28, Inc.2022—

What descends from it? (5)

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

NumberDeviceApplicantDecidedDescendants
K231231MR Safety and Compatibility Testing and Labeling for Paragon 28 Orthopedic Fixation…Paragon 28, Inc.20231
K221150Advanced Bone PlateDouble Medical Technology, Inc.20231
K233863TriMed ASET Foot Plating System (1ST MTP 9-hole Long Plate), TriMed ASET Foot Plating…TriMed, Inc.20240

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 3 years and passes through 1 company; a new generation was cleared every 1.5 years on median.
  • None of the 3 ancestors has a recall.
  • Of its descendants, K231231 (Paragon 28, Inc., 2023) has gone furthest, with 1 descendant of its own.

How does its category compare?

All HRS devices

HRS Plate, Fixation, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · HRS

54in 2025

2007: 352008: 352009: 472010: 492011: 432012: 592013: 562014: 762015: 562016: 442017: 572018: 402019: 462020: 482021: 402022: 472023: 402024: 542025: 542026 (partial year): 51
2007high 76 (2014) · low 35 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HRS

90in 2025

2007: 63 days median2008: 87 days median2009: 85 days median2010: 100 days median2011: 88 days median2012: 106 days median2013: 89 days median2014: 57 days median2015: 97 days median2016: 109 days median2017: 122 days median2018: 116 days median2019: 89 days median2020: 88 days median2021: 87 days median2022: 144 days median2023: 120 days median2024: 96 days median2025: 90 days median2026 (partial year): 82 days median
2007high 144 (2022) · low 57 (2014)2026

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

Recalls per year · HRS

1in 2025

2007: 22008: 112009: 32010: 162011: 52012: 42013: 112015: 72016: 52017: 32018: 22019: 252020: 12021: 92022: 32023: 12025: 12026 (partial year): 3
2007high 25 (2019) · low 0 (2014)2026

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

Adverse event reports per year · HRS

2,306in 2025

2007: 3392008: 3112009: 4352010: 4912011: 7732012: 1,6632013: 2,6432014: 2,4132015: 3,0952016: 2,2762017: 2,2202018: 2,6632019: 3,3592020: 2,7902021: 2,4422022: 1,7002023: 2,0492024: 1,8492025: 2,306
2007high 3,359 (2019) · low 311 (2008)2025

MAUDE reports naming product code HRS, 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
200735632339
2008358711311
200947853435
20104910016491
201143885773
20125910641,663
20135689112,643
2014765702,413
2015569773,095
20164410952,276
20175712232,220
20184011622,663
20194689253,359
2020488812,790
2021408792,442
20224714431,700
20234012012,049
2024549601,849
2025549012,306
202651823—

What is it indicated for?

The Baby Gorilla®/Gorilla® Bone Plates and Bone Screws of the Baby Gorilla®/Gorilla® Plating System are indicated for use in stabilization and fixation of fractures or osteotomies; intra and extra articular fractures, joint depression, and multi-fragmentary fractures; revision procedures, joint fusion and reconstruction of small bones of the toes, feet and ankles including the distal tibia, talus, and calcaneus, as well as the fingers, hands, and wrists.…

Read the full statement (379 words)

The Baby Gorilla®/Gorilla® Bone Plates and Bone Screws of the Baby Gorilla®/Gorilla® Plating System are indicated for use in stabilization and fixation of fractures or osteotomies; intra and extra articular fractures, joint depression, and multi-fragmentary fractures; revision procedures, joint fusion and reconstruction of small bones of the toes, feet and ankles including the distal tibia, talus, and calcaneus, as well as the fingers, hands, and wrists. The system can be used in both adult and pediatric patients. Specific examples include:

Forefoot:

* Arthrodesis of the first metatarsalcuneiform joint (Lapidus Fusion)

* Metatarsal or phalangeal fractures and osteotomies

* Lesser metatarsal shortening osteotomies (e.g. Weil)

* Fifth metatarsal fractures (e.g. Jones Fracture)

Mid/Hindfoot:

* LisFranc Arthrodesis and/or Stabilization

* 1st (Lapidus), 2nd, 3rd, 4th, and 5th Tarsometatarsal (TMT) Fusions

* Intercuneiform Fusions

*Navicular-Cuneiform (NC) Fusion

* Talo-Navicular (TN) Fusion

* Calcaneo-Cuboid (CC) Fusion

* Subtalar Fusion

* Medial Column Fusion

* Cuneiform Fracture

* Cuboid Fracture

*Navicular Fracture

Ankle:

* Lateral Malleolar Fractures

* Syndesmosis Injuries

* Medial Malleolar Fractures and Osteotomies

* Bi-Malleolar Fractures

* Tri-Malleolar Fractures

* Posterior Malleolar Fractures

* Distal Anterior Tibia Fractures

* Vertical Shear Fractures of the Medial Malleolus

* Pilon Fractures

* Distal Tibia Shaft Fractures

* Distal Fibula Shaft Fractures

* Distal Tibia Periarticular Fractures

* Medial Malleolar Avulsion Fractures

* Lateral Malleolar Avulsion Fractures

* Tibiotalocalcaneal Joint Arthrodesis

* Tibiotalar Joint Arthrodesis

* Tibiocalcaneal Arthrodesis

* Supramalleolar Osteotomy

* Fibular Osteotomy

First metatarsal osteotomies for hallux valgus correction including:

* Opening base wedge osteotomy

* Closing base wedge osteotomy

* Crescentic Osteotomy

* Proximal Osteotomy (Chevron and Rotational Oblique)

* Distal Osteotomy (Chevron/Austin)

Arthrodesis ofthe first metatarsophalangeal joint (MTP) including:

* Primary MTP Fusion due to hallux ridgidus and/or hallux valgus

* Revision MTP Fusion

* Revision of failed first MTP Arthroplasty implant

Flatfoot:

* Lateral Column Lengthening (Evans Osteotomy)

* Plantar Flexion Opening Wedge Osteotomy of the Medial Cuneiform (Cotton Osteotomy)

* Calcaneal Slide Osteotomy

Charcot:

* Medial column fusion (talus, navicular, cuneiform, metatarsal) for neuropathic osteoarthropathy (Charcot)

* Lateral column fusion (calcaneus, cuboid, metatarsal) for neuropathic osteoarthropathy (Charcot)

In addition, the non-locking, titanium screws and washers are indicated for use in bone reconstruction, osteotomy, arthrodesis, joint fusion, 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. “K222194: Baby Gorilla®/Gorilla® Plating System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K222194

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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