← Product Code [HRS](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HRS) · K163383 # GREENS BRAND Locking Bone Plates and Screws Osteosynthesis Plating System, GREENS BRAND Of DHS/Dynamic Condylar Plate Plating System (K163383) _Greens Surgicals Pvt. , Ltd. · HRS · Apr 19, 2017 · Orthopedic · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HRS/K163383 ## Device Facts - **Applicant:** Greens Surgicals Pvt. , Ltd. - **Product Code:** [HRS](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HRS.md) - **Decision Date:** Apr 19, 2017 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 888.3030 - **Device Class:** Class 2 - **Review Panel:** Orthopedic - **Attributes:** Therapeutic ## Intended Use GREENS BRAND Locking Bone Plates and Screws Osteosynthesis Plating System, GREENS Brand of DHS/ Dynamic Condylar Plates Plating System are provided non-sterile. GREENS BRAND Locking Bone Plates and Screws Osteosynthesis Plating System are indicated for treating fractures of various bones including the clavicle, pelvis, scapula, long bone ( humerus, ulna, radius, femur, tibia and fibula), and small bone (metacarpals, metatarsals, phalanges). GREENS Brand of DHS/ Dynamic Condylar Plating System is used to provide fixation of fractures to the proximal femur shaft and generally indicated for use in trochanteric, intertrochanteric fractures. The system is indicated for use in adult patients only. All implants are for single use only. ## Device Story System of metallic bone plates and screws for osteosynthesis; includes locking and non-locking variants. Inputs: patient anatomy and fracture site. Operation: plates contoured to bone anatomy; screws provide fixation via locking or compression mechanisms. Output: stabilized bone fractures. Used in clinical settings by orthopedic surgeons. Implants are non-sterile; require sterilization before use. Benefits: provides rigid fixation to facilitate bone healing in adult fracture patients. ## Clinical Evidence No clinical data. Substantial equivalence demonstrated through bench testing including static and dynamic four-point bend tests (ASTM F382, F384) for plates and torsional, driving torque, and pull-out tests (ASTM F543) for screws. ## Technological Characteristics Metallic bone plates and screws fabricated from stainless steel (ASTM F138, F139) and titanium alloy (ASTM F136). Plate thickness 1.0-6.0mm; hole count 2-22. Screw diameters 2.4-6.5mm. Mechanical fixation via locking or non-locking mechanisms. Supplied non-sterile; requires sterilization. ## Regulatory Identification Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system. ## Predicate Devices - Synthes 3.5mm LCP Elbow System ([K033995](/device/K033995.md)) - Synthes locking distal radius plating system ([K012114](/device/K012114.md)) - LCP Radial Head Plating System ([K040777](/device/K040777.md)) - Synthes Small Fragment Dynamic Compression Locking (DCL) System ([K000684](/device/K000684.md)) - Synthes (USA) 3.5 mm and 4.5 mm Locking Compression Plate ([K082807](/device/K082807.md)) - Synthes (USA) Medial Distal Tibia Plate ([K001945](/device/K001945.md)) - Synthes 3.5mm Titanium LCP Proximal Tibia Plate ([K030597](/device/K030597.md)) - Synthes LCP Proximal Tibia Plates ([K011978](/device/K011978.md)) - Synthes 4.5 mm LCP Straight Reconstruction Plate ([K051986](/device/K051986.md)) - Synthes Clavicle Hook Plate ([K061753](/device/K061753.md)) - Synthes (USA) 3.5mm LCP Periarticular Proximal Humerus Plates ([K082625](/device/K082625.md)) - Proximal Humerus Plate Long Synthes ([K041860](/device/K041860.md)) - Synthes 3.5mm LCP Clavicle Plate System ([K111540](/device/K111540.md)) - Synthes (USA) 2.7mm / 3.5mm LCP Anterolateral Distal Tibia Plate ([K092812](/device/K092812.md)) - Synthes (USA) 3.5 / 4.5mm LCP Medial Proximal Tibia Plate ([K032269](/device/K032269.md)) - Synthes (USA) 3.5mm LCP Posteromedial Proximal Tibia Plates ([K082628](/device/K082628.md)) - Synthes 2.7mm / 3.5mm LCP Distal Fibula Plate ([K073460](/device/K073460.md)) - Synthes LCP Distal Femur Plates ([K062564](/device/K062564.md)) - Synthes (USA) LCP Proximal Femur Plate and Screw ([K030858](/device/K030858.md)) - Synthes LCP Proximal Humerus Plates, Long ([K041860](/device/K041860.md)) - Synthes LCP Proximal Humerus Plates ([K011815](/device/K011815.md)) - Synthes Limited Contact-Dynamic Hip Screw Implant (LC-DHS) ([K923613](/device/K923613.md)) - Synthes Titanium Limited Contact-Dynamic Hip Screw Implant (Ti LC-DHS) ([K953607](/device/K953607.md)) - Synthes dynamic condylar screw or D.C.S. ([K840954](/device/K840954.md)) - Synthes 2.4mm/2.7mm variable angle LCP Forefoot/Midfoot System ([K100776](/device/K100776.md)) - Synthes Cortical Screws ([K112583](/device/K112583.md)) - Synthes Large Fragment Dynamic Compression Locking (DCL) System ([K000682](/device/K000682.md)) - Synthes (USA) 6.5 mm Cancellous Screws ([K061621](/device/K061621.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. Inside the circle is an abstract symbol that resembles a stylized caduceus or a representation of human figures. Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002 April 19, 2017 Greens Surgicals Pvt. Ltd. Dr. Vinay Kumar Director 209 (Second Floor), Saffron Complex Fatehgunj Vadodara, 390 002 IN Re: K163383 Trade/Device Name: GREENS BRAND Locking Bone Plates and Screws Osteosynthesis Plating System, GREENS BRAND of DHS/Dynamic Condylar Plates Plating System Regulation Number: 21 CFR 888.3030 Regulation Name: Single/multiple component metallic bone fixation appliances and accessories Regulatory Class: Class II Product Code: HRS. HWC Dated: November 21, 2016 Received: December 1, 2016 Dear Dr. Kumar: We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food. Drug. and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR {1}------------------------------------------------ Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical devicerelated adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance. You may obtain other general information on your responsibilities under the Act from the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Sincerely. # Lori A. Wiggins -S for Mark N. Melkerson Director Division of Orthopedic Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ # Indications for Use 510(k) Number (if known) # K163383 Device Name GREENS BRAND Locking Bone Plates and Screws Osteosynthesis Plating System, GREENS Brand of DHS/Dynamic Condylar Plate Plating System #### Indications for Use (Describe) GREENS BRAND Locking Bone Plates and Screws Osteosynthesis Plating System, GREENS Brand of DHS/Dynamic Condylar Plate Plating System are provided non-sterile. GREENS BRAND Locking Bone Plates and Screws Osteosynthesis Plating System are indicated for treating fractures of various bones including the clavis, scapula. long bone ( humerus, ulna, radius, femur, tibia and fibula), and small bone (metacarpals, metatarsals, phalanges). GREENS Brand of DHS/Dynamic Condylar Plate Plating System is used to provide fixation of fractures to the proximal femur shaft and generally indicated for use in trochanteric, intertrochanteric fractures. The system is indicated for use in adult patients only. All implants are for single use only. Type of Use (Select one or both, as applicable) > Prescription Use (Part 21 CFR 801 Subpart D) Over-The-Counter Use (21 CFR 801 Subpart C) # PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON A SEPARATE PAGE IF NEEDED. #### FOR FDA USE ONLY Concurrence of Center for Devices and Radiological Health (CDRH) (Signature) This section applies only to requirements of the Paperwork Reduction Act of 1995. #### *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.* The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to: > Department of Health and Human Services Food and Druq Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff(@fda.hhs.gov "An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number." {3}------------------------------------------------ Premarket Notification 510(k) Summary as required by Section 807.92 General Company Information as required by 807:92 (a) | (a.1) The submitter's name, address, telephone number, a contact person, and the date the summary | | | |---------------------------------------------------------------------------------------------------|--|--| | was prepared | | | | | | | Submitter's Name: GREENS SURGICALS PVT. LTD. Address: | | Office:
209 (Second Floor), Saffron Complex, Fatehgunj, Vadodara-390
002 (INDIA) | |----------------------|----------------------------------------------------------------------------------------| | | Factory:
Plot No. 508-512, Savli Industrial Estate, GIDC Manjusar, Vadodara - | | | 391775 Gujarat (INDIA) | | Contact Person Name: | Dr. Vinay Kumar | | Title: | Director | | Phone Number: | +91-2667 264 890 | | Dated: | 21-11-2016 | # This is a bundled submission. Throughout the submission there is a mention of GREENS BRAND Locking Bone Plates and Screws Osteosynthesis Plating System, GREENS Brand of DHS/ Dynamic Condylar Plates Plating System that represents the range of products covered under this 510(k) submission. {4}------------------------------------------------ ### a.2: The name of the device, including the trade or proprietary name if applicable, the common or usual name, and the classification name, if known ## Proprietary Name: - . GREENS BRAND Locking Bone Plates and Screws Osteosynthesis Plating System, GREENS Brand of DHS/ Dynamic Condylar Plates Plating System ## Common or Usual Name: - Orthopaedic Bone Plates - Orthopaedic Bone Screws #### Classification Name: - · PLATES, FIXATION, BONE - · SCREWS, FIXATION, BONE ### Product Code: HRS, HWC Device Class: ll Review Pane: Orthopaedic 21 CFR 888.3030 and 21 CFR 888.3040 Requlation Number: Further Description of GREENS BRAND Locking Bone Plates and Screws Osteosynthesis Plating System, GREENS Brand of DHS/ Dynamic Condylar Plates Plating System Generally there are following types of bone plates used with cortical (cortex) and Locking Screws. These bone plates are generally designed on the basis of the bone contour and anatomy. | S. No. | Type | Subtype | |--------|-----------------------------|-----------------------------------------------------------------------------------| | 01 | Small and Large
Fragment | T-Shaped, Hook, Angled Plates. Reconstructions plates. | | 02 | Dynamic compression | Small DCP, Narrow DCP, Lengthening Narrow, Broad
DCP, Lengthening Broad Plates | | 03 | Mini Fragment | T-Shaped | | 04 | Hip Plate | DHS / Dynamic Condylar Plates | CONFIDENTIAL {5}------------------------------------------------ # Variants/Types: GREENS BRAND Locking Bone Plates and Screws Osteosynthesis Plating System are further subdivided into following categories | S. No. | Category | Types | |--------|-------------------------------|------------------------------------| | 01 | Large Fragment Plates | Locking Version | | 02 | Small Fragment Plates | Locking Version | | 03 | Mini Fragment Plates | Locking Version | | 04 | DHS / Dynamic Condylar Plates | Locking and Non-Locking Version | | 05 | Bone Screws | Locking and Non-Locking
Version | # A3) Identification of the Predicate Device: Following are the predicate device 510(k) with which we are declaring substantial equivalence: Following is the range of variants covered with their corresponding predicate devices. | S. No. | Subject Device | Predicate Device | |-------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Mini
Fragment | | | | 01. | Locking Posterolateral Distal Humerus Plate
2.7/3.5mm | Synthes 3.5mm LCP Elbow System
(K033995) | | 02. | Locking Distal Dorsal Radius T-Plates 2.7mm | K012114 (Synthes locking distal radius
plating system) | | 03. | Locking Volar Distal Radius Plate Extra-Articular
Plates Ø 2.4mm/2.7mm Left and Right | LCP Radial Head Plating
System (K040777) | | 04. | 3.5MM Small Locking T- Plate 3.5mm | Synthes Small Fragment Dynamic
Compression Locking( DCL)
System(K000684) | | Small
Fragment | | | | 05. | 3.5mm Locking Plate | K082807 Synthes (USA) 3.5 nun and
4.5 nun Locking Compression Plate | | 06. | Locking Medial Distal Tibia Plate 3.5mm /
4.0mm Left & Right | Synthes (USA) Medial Distal Tibia
Plate (K001945) | | 07. | 3.5mm Locking T- Plate Oblique Angled, Left&
Right | Synthes Small Fragment Dynamic
Compression Locking( DCL) System
(K000684) | | 08. | 3.5MM Locking T-Plate Right Angle | Synthes Small Fragment Dynamic
Compression Locking( DCL)
System(K000684) | | 09. | 3.5MM Locking Proximal Tibia Plate, Left& Right | Synthes 3.5mm Titanium LCP
Proximal Tibia Plate (K030597) OR
Synthes LCP Proximal Tibia Plates
(K011978) | | 10. | 3.5mm Locking Reconstruction Plate | Synthes 4.5 mm LCP Straight
Reconstruction Plate (K051986) | | 11. | Locking Clavicle Hook Plate Ø 3.5mm, Left &
Right | Synthes Clavicle Hook Plate
(K061753) | | 12. | 3.5mm Locking Periarticular Proximal Humerus
Plate, Left and Right | Synthes (USA) 3.5mm LCP
Periarticular Proximal Humerus Plates
(K082625) | | 13. | 3.5MM Locking Proximal Humerus Plate | Proximal Humerus Plate Long
Synthes K041860 | | 14. | 3.5MM Locking Superior Anterior Clavicle
Plates, Left and Right | Synthes 3.5mm LCP Clavicle Plate
System (K111540) | | 15. | 3.5MM Locking Anterolateral Distal Tibia Plate,
Left and Right | Synthes (USA) 2.7mm / 3.5mm LCP
Anterolateral Distal Tibia Plate
(k092812) | | 16. | 3.5MM Locking Medial Proximal Tibia Plate Left
and Right | Synthes (USA) 3.5 / 4.5mm LCP®
Medial Proximal Tibia Plate (K032269) | | 17. | 3.5mm Locking Posteromedial Proximal Tibia
Plate Right and Left | Synthes (USA) 3.5mm LCP
Posteromedial Proximal Tibia Plates
(K082628) | | 18. | 3.5MM Locking Distal Fibula Plate, Left and
Right | Synthes 2.7mm / 3.5mm LCP Distal
Fibula Plate (K073460) | | Large
Fragment | | | | 19. | Narrow Locking Plate Ø 4.5mm/5.0mm Screws | Synthes 3.5 and 4.5mm Locking
Compression Plate System (K082807) | | 20. | Locking Reconstruction Plate, Ø 4.5mm | Synthes 4.5 mm LCP Straight
Reconstruction Plate (K051986) | | 21. | Broad Locking Plate Ø 4.5mm/5.0mm Screws | Synthes 3.5 and 4.5mm Locking Compression Plate System (K082807) | | 22. | Locking Distal Femur Plate, Right
Locking Distal Femur Plate, Left | Synthes LCP Distal Femur Plates (K062564) | | 23. | Proximal Lateral Tibia Locking Plate, Left
Proximal Lateral Tibia Locking Plate. Right | Synthes LCP Proximal Tibia Plate (K011978) | | 24. | Locking Proximal Femur Plate 4.5/5.0/6.5mm
Left & Right | Synthes (USA) LCP Proximal Femur Plate and Screw (K030858) | | 25. | Locking Philos Proximal Humeral Plate - Long

Locking Philos Proximal Humeral Plate - Short | Synthes (USA) LCP® Proximal Humerus Plates, Long (K041860)

Synthes LCP Proximal Humerus Plates K011815 | | 26. | Broad LC DCP Plate, 4.5mm | Synthes 3.5 and 4.5mm Locking Compression Plate System (K082807) | | 27. | Narrow LC DCP Plate 4.5mm | Synthes 3.5 and 4.5mm Locking Compression Plate System (K082807) | | 28. | Dynamic Hip Screw (Non-Locking) Plate (with Dynamic Compression Holes) (Long Barrel)

Dynamic Hip Screw (Non-Locking) Plate (with Dynamic Compression Holes) (Short Barrel) | Synthes Limited Contact-Dynamic Hip Screw Implant (LC-DHS)" for K923613

Synthes Titanium Limited Contact-Dynamic Hip Screw Implant (Ti LC-DHS)" for K953607 | | 29. | Dynamic Condylar Plate with Dynamic Compression Holes (Barrel length 25 mm) | Synthes dynamic condylar screw or D.C.S. K840954 | | 30. | Dynamic Hip Screw, Ø 12.5mm with Compression Screw | Synthes Limited Contact-Dynamic Hip Screw Implant (LC-DHS)" for K923613

Synthes Titanium Limited Contact-Dynamic Hip Screw Implant (Ti LC-DHS) for K953607 | | | Locking and
Non-Locking
Screw | | | 31. | Locking Head Screw, Ø 2.4mm - Self Tapping | Synthes Locking Distal Radius Plating System (K012114) | | 32. | Locking Head Screw, Ø 2.7mm - Self Tapping | Synthes 2.4mm/2.7mm variable angle LCP Forefoot/Midfoot System K100776 | | 33. | Locking Head Screw, Ø 3.5mm - Self Tapping | Synthes Small Fragment Dynamic | | | | Compression Locking (DCL) System
(K000684) | | 34. | Cortex Screw Ø 3.5mm, Self Tapping | Synthes Cortical Screws K112583 | | 35. | Cortex Screw Ø 4.5mm, Self Tapping | Synthes Cortical Screws K112583 | | 36. | Locking Head Screw, Ø 5.0mm - Self Tapping | Synthes Large Fragment Dynamic
Compression Locking (DCL) System
(K000682) | | 37. | Cancellous Screw, Ø6.5mm, 16mm Thread,
32mm Thread and Full Thread | Synthes (USA) 6.5 mm Cancellous
Screws (K061621) | {6}------------------------------------------------ {7}------------------------------------------------ CONFIDENTIAL {8}------------------------------------------------ # a4). A description of the device that is the subject of the premarket notification submission, such as might be found in the labeling or promotional material for the device # Device Description: GREENS BRAND Locking Bone Plates and Screws Osteosynthesis Plating System, GREENS Brand of DHS/ Dynamic Condylar Plates Plating System consists of various shape and sizes of plates featuring compression and locking holes, full-threaded-cortical, locking self-tapping screws, compression and dynamic screws. The plates and screws are fabricated from Stainless Steel And Titanium. The system contains several models based on the size of the device and application site such as fixation/reconstruction of small fragment bones, forefoot, mid-foot, rear-foot, ankle, or other bones appropriate for the size of the device. The plate implants are in many models available: like, Reconstruction Plates, T- Plates, , Anatomical Plates, Clavicle Hook Plates. These all are mainly divided into - Large Fragment Plates - Small Fragment Plates ● - Mini Fragment Plates - Hip Plates (DHS and Dynamic Condylar Plate) The thickness of the plates varies from 1.0mm to 6mm; and the number of the holes varies from 2 to 22. The Locking screw implants are in corresponding diameter ranges from 2.4mm, 2.7mm, 3.5mm, 5.0mm diameters with lengths varying as per the requirements and minimum length: 6 mm to maximum length 90mm The Non-locking screw implants are in 3.5mm and 4.5mm diameter and length range from 10mm to 140mm. #### These implants are supplied non-sterile, the products have to be sterilized prior to use. {9}------------------------------------------------ ### A5). A statement of the intended use of the device ### Indications for Use: GREENS BRAND Locking Bone Plates and Screws Osteosynthesis Plating System, GREENS Brand of DHS/ Dynamic Condylar Plates Plating System are provided non-sterile. GREENS BRAND Locking Bone Plates and Screws Osteosynthesis Plating System are indicated for treating fractures of various bones including the clavicle, pelvis, scapula, long bone ( humerus, ulna, radius, femur, tibia and fibula), and small bone (metacarpals, metatarsals, phalanges). GREENS Brand of DHS/ Dynamic Condylar Plating System is used to provide fixation of fractures to the proximal femur shaft and generally indicated for use in trochanteric, intertrochanteric fractures. The system is indicated for use in adult patients only. All implants are for single use only. # a6). Summary of Technological Characteristics as compared to the predicate devices: ### Substantial equivalence including comparison with predicate devices A comparison between the GREENS BRAND Locking Bone Plates and Screws Osteosynthesis Plating System, GREENS Brand of DHS/ Dynamic Condylar Plates Plating System and predicate devices has been performed which has resulted in demonstration of similarities in dimensional and performance criteria. ### Following is the summary of parameters in which the comparison has been verified: | S. No. | Characteristics | Predicate Device Versus New
Device (GREENS Brand) | Remarks | |--------|-----------------------------|-------------------------------------------------------------------------------------|------------| | 01 | Indications for use | Similar intended use in New Device and
Predicate device | Equivalent | | 02 | Material | Same material used in New Device and
Predicate device | Equivalent | | 03 | Performance
Standards | Same performance standards used in both
New Device as well as predicate device | Equivalent | | 04 | Sterilization | Same method of sterilization used in both
New Device as well as Predicate device | Equivalent | | 05 | Dimensional
Verification | Same dimensions found in both New
Device as well as Predicate device | Equivalent | {10}------------------------------------------------ ### b1). Discussion on the non-clinical testing performed Following are the applicable product standards considered for non-clinical standards - A: Material Standards - B: Performance Standards ## A: Material Standards: The material standards are the essential part to be complied to first, as it is the basis of manufacturing metallic surgical implants. We have complied to following material standards - 1. ASTM F 136: Standard specification for wrought Titanium-6Aluminium-4Vanadium ELI (Extra low interstitial) Alloy for surgical implant applications. - 138: Standard Specification for Wrought 18 chromium-14Nickel-2. ASTM F 2.5Molybdenum stainless steel bar and wire for surgical implants. - 3. ASTM F 139: Standard Specification for Wrought 18Chromium-14Nickel-2.5Molybdenum Stainless Steel Sheet and Strip for Surgical Implants We have verified the purchased material compliance to these standards and copies of the relevant test results were provided in the submission. ### B: Performance Standards: The device performance of GREENS BRAND Locking Bone Plates and Screws Osteosynthesis Plating System, GREENS Brand of DHS/ Dynamic Condylar Plates Plating System has been demonstrated against following applicable standards - · ASTM F 382, - ASTM F 384 and - · ASTM F 543. #### For Bone Plates: As per ASTM F 382 and ASTM F 384 Static Four Point Bend Test: Conforms, Dynamic Four Point Bend Test: Conforms #### For Bone Screws: As per ASTM F 543 : Torsional Properties: Conforms, Driving Torque : Conforms, Pull-out Test: Conforms {11}------------------------------------------------ #### b2). Discussion on the clinical evaluation referenced and relied upon: GREENS BRAND Locking Bone Plates and Screws Osteosynthesis Plating System, GREENS Brand of DHS/ Dynamic Condylar Plates Plating System are of similar design and pattern as well as similar intended use. Clinical information was not necessary to demonstrate substantial equivalence. #### CONCLUSION: #### General, Safety and Performance conclusion: From the available data available we can justify that the GREENS BRAND Locking Bone Plates and Screws Osteosynthesis Plating System, GREENS Brand of DHS/ Dynamic Condylar Plates Plating System are as safe, as effective and perform as same indications for use as that of already marketed predicate devices identified in a3. of 510(k) summary. Hence these devices can be considered safe and effective for their intended use. --- **Source:** [https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HRS/K163383](https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HRS/K163383) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com