Implacil Implant System

K202832 · Implacil DE Bortoli Material Odontologico Ltda · DZE · May 26, 2021 · Dental

Device Facts

• Record ID: K202832
• Device Name: Implacil Implant System
• Applicant: Implacil DE Bortoli Material Odontologico Ltda
• Product Code: DZE · Dental
• Decision Date: May 26, 2021
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 872.3640
• Device Class: Class 2
• Attributes: Therapeutic

Intended Use

Implacil Implant System is intended for placement in the maxillary or mandibular arch to provide support for single-unit and/or multi-unit restorations. When a one-stage surgical approach is applied, the Implant System is intended for immediate loading when good primary stability is achieved and with appropriate occlusal loading.

Device Story

Threaded, self-tapping, root-form endosseous dental implants; used to support single or multiple dental restorations; placed in maxillary or mandibular arch; available in External Hex (HE), Internal Hex (HI), and Morse Taper (CM AR) connections; features radial chambers on external surface; made of Grade 4 commercially pure titanium; surface treated via abrasive particle jet and acid etching; used by dental professionals in clinical settings; provides structural support for prosthetic components; benefits patients by restoring chewing function.

Clinical Evidence

No clinical data were included in this submission. Substantial equivalence is supported by bench testing and design comparisons.

Technological Characteristics

Material: Commercially pure titanium (Grade 4) per ASTM F67. Design: Threaded, root-form, bone-level implants with HE, HI, or CM AR connections. Surface: Grit-blasted and acid-etched with radial chambers. Sterilization: Irradiation. Dimensions: Various diameters (3.5-5.0 mm) and lengths (7-15 mm).

Indications for Use

Indicated for patients requiring dental implants in the maxillary or mandibular arch for single or multi-unit restorations; supports immediate loading protocols when primary stability and occlusal conditions are met.

Regulatory Classification

Identification

An endosseous dental implant is a prescription device made of a material such as titanium or titanium alloy that is intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as artificial teeth, in order to restore a patient's chewing function.

Special Controls

*Classification.* (1) Class II (special controls). The device is classified as class II if it is a root-form endosseous dental implant. The root-form endosseous dental implant is characterized by four geometrically distinct types: Basket, screw, solid cylinder, and hollow cylinder. The guidance document entitled “Class II Special Controls Guidance Document: Root-Form Endosseous Dental Implants and Endosseous Dental Implant Abutments” will serve as the special control. (See § 872.1(e) for the availability of this guidance document.)(2) *Classification.* Class II (special controls). The device is classified as class II if it is a blade-form endosseous dental implant. The special controls for this device are:(i) The design characteristics of the device must ensure that the geometry and material composition are consistent with the intended use; (ii) Mechanical performance (fatigue) testing under simulated physiological conditions to demonstrate maximum load (endurance limit) when the device is subjected to compressive and shear loads; (iii) Corrosion testing under simulated physiological conditions to demonstrate corrosion potential of each metal or alloy, couple potential for an assembled dissimilar metal implant system, and corrosion rate for an assembled dissimilar metal implant system; (iv) The device must be demonstrated to be biocompatible; (v) Sterility testing must demonstrate the sterility of the device; (vi) Performance testing to evaluate the compatibility of the device in a magnetic resonance (MR) environment; (vii) Labeling must include a clear description of the technological features, how the device should be used in patients, detailed surgical protocol and restoration procedures, relevant precautions and warnings based on the clinical use of the device, and qualifications and training requirements for device users including technicians and clinicians; (viii) Patient labeling must contain a description of how the device works, how the device is placed, how the patient needs to care for the implant, possible adverse events and how to report any complications; and (ix) Documented clinical experience must demonstrate safe and effective use and capture any adverse events observed during clinical use.

Predicate Devices

• Implacil Implant System (K183024)

Reference Devices

• S.I.N. Dental Implant System (K170392)
• DSP Implant System (K192839)

Submission Summary (Full Text)

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Implacil de Bortoli Material Odontologico Ltda Thiago Toni Quality Manager Rua Vicente de Carvalho 178-182 Sao Paulo, Sao Paulo 01521020 BRAZIL

Re: K202832

Trade/Device Name: Implacil Implant System Regulation Number: 21 CFR 872.3640 Regulation Name: Endosseous Dental Implant Regulatory Class: Class II Product Code: DZE Dated: April 19, 2021 Received: April 29, 2021

Dear Thiago Toni:

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. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. 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.

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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 Part 807); labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

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 https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.

For comprehensive regulatory information about medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email ([e-mail]) or phone [phone] or 301-796-7100).

Sincerely.

Andrew I. Steen Assistant Director DHT1B: Division of Dental and ENT Devices OHT1: Office of Ophthalmic, Anesthesia, Respiratory, ENT and Dental Devices Office of Product Evaluation and Ouality Center for Devices and Radiological Health

Enclosure

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# Indications for Use

510(k) Number (if known) K202832

Device Name Implacil Implant System

#### Indications for Use (Describe)

Implacil Implant System is intended for placement in the maxillary or mandibular arch to provide support for single-unit and/or multi-unit restorations. When a one-stage surgical approach is applied, the Implant System is intended for immediate loading when good primary stability is achieved and with appropriate occlusal loading.

| Type of Use (Select one or both, as applicable) | <span> <span style="font-size: 16px;">☑</span> Prescription Use (Part 21 CFR 801 Subpart D) </span> <span> ☐ Over-The-Counter Use (21 CFR 801 Subpart C) </span> |
|-------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
|-------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------|

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#### 510(k) Summary

#### ADMINISTRATIVE INFORMATION

| Sponsor | Implacil de Bortoli Material Odontologico Ltda<br>Rua Vicente de Carvalho 178-182<br>São Paulo, São Paulo, Brazil 01521020<br>Telephone: [phone] |
|--------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Contact Person | Thiago Toni<br>Quality Manager<br>[e-mail] |
| Date Prepared | 25/May/2021 |
| DEVICE NAME AND CLASSIFICATION | |
| Trade/ Proprietary Name<br>Common Name | Implacil Implant System<br>Dental implant and abutment |
| Regulation Number<br>Regulation Name<br>Regulation Class<br>Product Code | 21 CFR 872.3640<br>Endosseous dental implant<br>Class II<br>DZE |
| Classification Panel<br>Reviewing Branch | Dental Products Panel<br>Dental Devices Branch |
| PREDICATE DEVICE INFORMATION | |
| Primary Predicate Device | K183024 - Implacil Implant System - Implacil de Bortoli Material<br>Odontologico Ltda |
| Reference Devices | K170392 - S.I.N. Dental Implant System - S.I.N. Sistema de Implante<br>Nacional S.A.<br>K192839 - DSP Implant System - D.S.P. Industrial Fireli |

#### INDICATIONS FOR USE

Implacil Implant System is intended for placement in the maxillary or mandibular arch to provide support for single-unit and/or multi-unit restorations. When a one-stage surgical approach is applied, the Implacil Implant System is intended for immediate loading when good primary stability is achieved and with appropriate occlusal loading.

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### SUBJECT DEVICE DESCRIPTION

The Maestro line of Implacil Implant System is composed of three implant-to-abutment connections which are External Hex (HE), Internal Hex (HI) and Morse Taper AR Due Cone (CM AR). All of them are bone-level implants.

The implants subject of this submission are threaded, self-tapping, root form endosseous dental implants used to support single or multiple restorations in immediate or conventional loading protocols. The subject devices are recommended for all bone density types, depending on the drill sequence used.

The implants are made of commercially pure titanium (Grade 4) conforming to ASTM F67 and are surface treated to create a rough surface using an abrasive particle jet concept with controlled grain oxides, followed by acid etching creating uniform cavities in the implant surface. The Maestro implant line has radial channels (55 °) or chambers on their external surface.

HE implants are available in tapered (conical) root-forms designs in three diameters and platforms (3.5, 4.0 and 5.0 mm). For implants diameter 3.5, there are eight available lengths (8, 9, 10, 11, 12, 13, 14, 15), while for diameters 4.0 and 5.0 there are nine lengths ( 7, 8, 9, 10, 11, 12, 13, 14, 15).

HI implants are available in tapered (conical) root-forms designs in three diameters and platforms (3.5, 4.0 and 5.0 mm). For implants diameter 3.5, there are eight available lengths (8, 9, 10, 11, 12, 13, 14, 15), while for diameters 4.0 and 5.0 there are nine lengths (7, 8, 9, 10, 11, 12, 13, 14, 15).

CM AR implants are available in tapered (conical) root-form design, in four diameters (3.5, 4.0, 4.5 and 5.0 mm). For implants diameter 3.5, there are eight available lengths (8, 9, 10, 11, 12, 13, 14, 15), while for diameters 4.0, 4.5 and 5.0 there are nine lengths (7, 8, 9, 10, 11, 12, 13, 14, 15).

The compatible prosthetic components mate exclusively with the subject implants of the same implant-toabutment interface (HJ, HE, CM AR). All the compatible prosthetic components were cleared under K183024.

# TECHNOLOGICAL CHARACTERISTICS

The subject device and the predicate devices have the same intended use and similar technological characteristics as shown in the tables below. Differences in the design features between the subject devices and the primary predicate device K183024 are addressed by comparison to the reference devices in design and range of dimensions.

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| | SUBJECT DEVICE | PRIMARY PREDICATE DEVICE | REFERENCE DEVICE | Substantial Equivalence Discussion | |
|---------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Trade Name<br>Information | K202832 - Implacil Implant System<br>Implacil de Bortoli Material Odontologico<br>Ltda | K183024 – Implacil Implant System<br>Implacil de Bortoli Material Odontologico<br>Ltda | K192839 - DSP Implant System<br>D.S.P. Industrial Eireli | | |
| Indication for Use | Implacil Implant System is intended for<br>placement in the maxillary or mandibular<br>arch to provide support for single-unit<br>and/or multi-unit restorations. When a<br>one-stage surgical approach is applied, the<br>Implacil Implant System is intended for<br>immediate loading when good primary<br>stability is achieved and with appropriate<br>occlusal loading. | Implacil Implant System is intended for<br>placement in the maxillary or mandibular<br>arch to provide support for single-unit<br>and/or multi-unit restorations. When a<br>one-stage surgical approach is applied, the<br>Implacil Implant System is intended for<br>immediate loading when good primary<br>stability is achieved and with appropriate<br>occlusal loading. | The DSP Implant System is intended to be<br>surgically placed in the bone of the upper or<br>lower jaw to provide support for prosthetic<br>devices, such as artificial teeth, to restore<br>chewing function. It may be used with single<br>stage or two-stage procedures, for single or<br>multiple unit restorations, and may be<br>loaded immediately when good primary<br>stability is achieved and with appropriate<br>occlusal loading. | Identical<br><br>The indication for use statement is<br>identical to the primary predicate device<br>and is within the scope of the reference<br>device. | |
| Implant-to-<br>abutment<br>connection | HE interface | HE interface<br>HI interface<br>Conical connection (CM AR) | HE interface | Identical<br><br>To the primary predicate and reference<br>devices. | |
| Raw Material | CPTi | CPTi | CPTi | Identical<br><br>To the primary predicate and reference<br>devices. | |
| Surface | Grit-blasted and acid-etched<br><br>Machined collar: h 1.0 mm | Grit-blasted and acid-etched<br><br>Machined collar: h 1.0 mm | Grit-blasted and acid-etched.<br><br>Machined collar: h 1.0 mm | Equivalent<br><br>Identical to the primary predicate and<br>reference devices. | |
| Design - presence of<br>chambers | Yes | No | No | Different<br><br>The presence of chambers in the external<br>surface is the only difference between the<br>subject and primary predicate device<br>design. The substantial equivalence is<br>supported by external surface area<br>comparison. No impact in mechanical<br>performance is expected | |
| | SUBJECT DEVICE | PRIMARY PREDICATE DEVICE | REFERENCE DEVICE | | |
| Trade Name<br>Information | K202832 - Implacil Implant System | K183024 – Implacil Implant System | K192839 - DSP Implant System | Substantial Equivalence Discussion | |
| | Implacil de Bortoli Material Odontologico | Implacil de Bortoli Material Odontologico | D.S.P. Industrial Eireli | | |
| | Ltda | Ltda | | | |
| Implant diameter:<br>lengths (mm) | 3.5: 8, 9, 10, 11, 12, 13, 14, 15 | 3.3: 8, 10, 11.5, 13, 15 | 3.3: 8.5, 10, 11.5, 13, 15, 17 | Equivalent<br><br>Within the range of dimensions of the<br>primary predicate and reference devices. | |
| | | 3.5: 7, 9, 11, 13, 15 | 3.8: 8.5, 10, 11.5, 13, 15 | | |
| | 4.0: 7, 8, 9, 10, 11, 12, 13, 14, 15 | 3.75: 8, 10, 11.5, 13, 15 | | | |
| | | 4.0: 7, 8, 9, 10, 11, 11.5, 13, 15 | 4.3: 8.5, 10, 11.5, 13, 15 | | |
| | | 4.75: 8, 10, 11.5, 13, 15 | | | |
| | 5.0: 7, 8, 9, 10, 11, 12, 13, 14, 15 | 5.0: 7, 9, 11, 13, 15 | 5.0: 8.5, 10, 11.5, 13, 15 | | |
| | | | | | |
| Sterilization | Provided sterile by irradiation | Provided sterile by irradiation | Provided sterile by irradiation | Identical<br><br>To the primary predicate and reference<br>devices. | |
| | SUBJECT DEVICES | PRIMARY PREDICATE DEVICE | REFERENCE DEVICES | | |
| Trade Name<br>Information | K202832 - Implacil Implant System | K183024 - Implacil Implant System | K170392- S.I.N. Dental Implant<br>System | K192839 - DSP Implant System | Substantial Equivalence<br>Discussion |
| | Implacil de Bortoli Material<br>Odontologico Ltda | Implacil de Bortoli Material<br>Odontologico Ltda | S.I.N. Sistema de Implante<br>Nacional S.A. | D.S.P. Industrial Eireli | |
| Indication for Use | Implacil Implant System is<br>intended for placement in the<br>maxillary or mandibular arch to<br>provide support for single-unit<br>and/or multi-unit restorations.<br>When a one-stage surgical<br>approach is applied, the Implacil<br>Implant System is intended for<br>immediate loading when good<br>primary stability is achieved and<br>with appropriate occlusal<br>loading. | Implacil Implant System is<br>intended for placement in the<br>maxillary or mandibular arch to<br>provide support for single-unit<br>and/or multi-unit restorations.<br>When a one-stage surgical<br>approach is applied, the Implacil<br>Implant System is intended for<br>immediate loading when good<br>primary stability is achieved and<br>with appropriate occlusal loading. | S.I.N. Dental Implant System is<br>intended for placement in the<br>maxillary or mandibular arch to<br>provide support for single-unit or<br>multi-unit restorations. When a<br>one-stage surgical approach is<br>applied, the S.I.N. Dental Implant<br>System is intended for immediate<br>loading when good primary<br>stability is achieved and with<br>appropriate occlusal loading.<br>Implants with lengths less than 7<br>mm are intended for delayed<br>loading only. | The DSP Implant System is<br>intended to be surgically placed<br>in the bone of the upper or<br>lower jaw to provide support for<br>prosthetic devices, such as<br>artificial teeth, to restore<br>chewing function. It may be used<br>with single stage or two-stage<br>procedures, for single or multiple<br>unit restorations, and may be<br>loaded immediately when good<br>primary stability is achieved and<br>with appropriate occlusal<br>loading. | Identical<br><br>The indication for use statement<br>is identical to the primary<br>predicate device and is within the<br>scope of the reference devices. |
| Implant-to-<br>abutment<br>connection | HI interface | HE interface<br>HI interface<br>Conical connection (CM AR) | Conical connection (CM) | HE interface | Identical<br><br>To the primary predicate device. |
| Raw Material | CPTi | CPTi | CPTi | CPTi | Identical<br><br>To the primary predicate and<br>reference devices. |
| Surface | Grit-blasted and acid-etched<br><br>Machined collar: h 1.0 mm | Grit-blasted and acid-etched<br><br>Machined collar: h 1.0 mm | Grit-blasted and acid-etched | Grit-blasted and acid-etched<br><br>Machined collar: h 1.0 mm | Identical<br><br>To the primary predicate and<br>reference devices for the grit-<br>blasted and acid-etched surface<br>and identical to the primary<br>predicate and reference device<br>K192839 for the machined collar<br>height |

# Table 5.1: SE comparison on Maestro HE implants

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K202832- Implacil Implant System

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# Table 5.2: SE comparison on Maestro HI implants

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### K202832- Implacil Implant System

| | SUBJECT DEVICES | | PRIMARY PREDICATE DEVICE | | REFERENCE DEVICES | | |
|-----------------------------------|---------------------------------------------------|--|---------------------------------------------------|--|---------------------------------------------|---------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Trade Name<br>Information | K202832 - Implacil Implant System | | K183024 - Implacil Implant System | | K170392- S.I.N. Dental Implant<br>System | K192839 - DSP Implant System | Substantial Equivalence<br>Discussion |
| | Implacil de Bortoli Material<br>Odontologico Ltda | | Implacil de Bortoli Material<br>Odontologico Ltda | | S.I.N. Sistema de Implante<br>Nacional S.A. | D.S.P. Industrial Eireli | |
| Design - presence of<br>chambers | Yes | | No | | No | No | Different |
| | | | | | | | The presence of chambers in the<br>external surface is only difference<br>between the subject and primary<br>predicate device design. The<br>substantial equivalence is<br>supported by external surface<br>area comparison. No impact in<br>mechanical performance is<br>expected. |
| Implant diameter:<br>lengths (mm) | | | | | 2.9: 10, 11.5, 13 | | Equivalent |
| | | | 3.3: 8, 9, 11, 13, 15 | | | 3.3: 8.5, 10, 11.5, 13, 15, 17 | |
| | 3.5: 8, 9, 10, 11, 12, 13, 14, 15 | | 3.5: 8, 9, 11, 13, 15 | | 3.5: 8.5, 10, 11.5, 13, 15 | | Within the range of dimensions |
| | | | 3.75: 7, 9, 11, 13, 15 | | 3.8: 8.5, 10, 11.5, 13, 15 | 3.8: 8.5, 10, 11.5, 13, 15 | of the primary predicate and |
| | 4.0: 7, 8, 9, 10, 11, 12, 13, 14, 15 | | 4.0: 8, 9, 11, 13, 15 | | 4.0: 5, 6, 7 | 4.3: 8.5, 10, 11.5, 13, 15 | reference devices. |
| | | | 4.3: 7, 9, 11, 13, 15 | | 4.3: 8.5, 10, 11.5, 13, 15 | | |
| | | | 4.75: 7, 9, 11, 13, 15 | | 4.5: 8.5, 10, 11.5, 13, 15 | 5.0: 8.5, 10, 11.5, 13, 15 | |
| | 5.0: 7, 8, 9, 10, 11, 12, 13, 14, 15 | | 5.0: 7, 9, 11, 13, 15 | | 5.0: 5, 6, 7, 8.5, 10, 11.5, 13, 15 | | |
| Sterilization | Provided sterile by irradiation | | Provided sterile by irradiation | | Provided sterile by irradiation | Provided sterile by irradiation | Identical |
| | | | | | | | To the primary predicate and<br>reference devices. |

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| | SUBJECT DEVICE | PRIMARY PREDICATE DEVICE | REFERENCE DEVICE | |
|---------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Trade Name<br>Information | K202832 - Implacil Implant System<br>Implacil de Bortoli Material Odontologico<br>Ltda | K183024 – Implacil Implant System<br>Implacil de Bortoli Material Odontologico<br>Ltda | K170392- S.I.N. Dental Implant System<br>S.I.N. Sistema de Implante Nacional S.A. | Substantial Equivalence Discussion |
| Indication for Use | Implacil Implant System is intended for<br>placement in the maxillary or mandibular<br>arch to provide support for single-unit<br>and/or multi-unit restorations. When a<br>one-stage surgical approach is applied, the<br>Implacil Implant System is intended for<br>immediate loading when good primary<br>stability is achieved and with appropriate<br>occlusal loading. | Implacil Implant System is intended for<br>placement in the maxillary or mandibular<br>arch to provide support for single-unit<br>and/or multi-unit restorations. When a one-<br>stage surgical approach is applied, the<br>Implacil Implant System is intended for<br>immediate loading when good primary<br>stability is achieved and with appropriate<br>occlusal loading. | S.I.N. Dental Implant System is intended for<br>placement in the maxillary or mandibular<br>arch to provide support for single-unit or<br>multi-unit restorations. When a one-stage<br>surgical approach is applied, the S.I.N.<br>Dental Implant System is intended for<br>immediate loading when good primary<br>stability is achieved and with appropriate<br>occlusal loading. Implants with lengths less<br>than 7 mm are intended for delayed loading<br>only. | Equivalent<br><br>The indication for use statement is<br>identical to the primary predicate device<br>and within the scope of the reference<br>device. |
| Implant-to-<br>abutment<br>connection | Conical connection (CM AR)…