KLOCKNER DENTAL IMPLANT ABUTMENTS

K122988 · SOADCO, S.L. · NHA · Jul 19, 2013 · Dental

Device Facts

• Record ID: K122988
• Device Name: KLOCKNER DENTAL IMPLANT ABUTMENTS
• Applicant: SOADCO, S.L.
• Product Code: NHA · Dental
• Decision Date: Jul 19, 2013
• Decision: SESE
• Submission Type: Abbreviated
• Regulation: 21 CFR 872.3630
• Device Class: Class 2

Intended Use

The Klockner Dental Implant Abutments are intended to be placed into dental implants to provide support for prosthetic reconstructions such as crowns, bridges or overdentures. The Klockner Dental Implant Abutments include healing caps, temporary abutments, angled abutments, straight abutments, and overdentures. All abutments are intended to be used with the Klockner Dental Implant Systems, models: Essential ES, Essential ES, Essential ECK, Essential EC 1.5, SK2 and NK2.

Device Story

Klockner Dental Implant Abutments are prosthetic components placed into dental implants to facilitate rehabilitation. Components include healing caps (soft tissue healing), protective caps (impression protection), temporary abutments (provisional restoration support), angled/straight abutments (definitive prosthesis retention), and overdenture abutments (removable prosthesis retention). Inputs are the dental implant interface; outputs are the mechanical support for dental prostheses. Used in dental clinics by dentists/specialists. Straight abutments include a Titanium Base for CAD/CAM systems (e.g., 3M ESPE Lava). The device provides a stable connection between the endosseous implant and the final or provisional restoration, benefiting patients by restoring masticatory function and esthetics.

Clinical Evidence

No clinical data are presented in this submission. Substantial equivalence is supported by bench testing, including bioburden and sterility testing (ISO 11737-1/17665-1) and mechanical performance testing (torsion and fatigue per ISO 14801).

Technological Characteristics

Materials: Titanium Alloy (ASTM F136), Titanium cp (ASTM F67), PMMA, POM C. Features: Internal/external octagonal connections, ball attachments, angled (15°-30°) and straight designs. Includes Titanium Base for CAD/CAM. Sterilization: Validated per ISO 17665-1. Connectivity: Mechanical interface for dental prosthetics; CAD/CAM compatible.

Indications for Use

Indicated for patients requiring prosthetic reconstruction (crowns, bridges, or overdentures) supported by Klockner Dental Implant Systems (models: Essential ES, ECK, EC 1.5, SK2, NK2).

Regulatory Classification

Identification

An endosseous dental implant abutment is a premanufactured prosthetic component directly connected to the endosseous dental implant and is intended for use as an aid in prosthetic rehabilitation.

Special Controls

*Classification.* Class II (special controls). 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.)

Predicate Devices

• Klockner Essential Dental Implant System, models: EC, ES, ECK (K080224)
• Klockner Essential Dental Implant System, model: EC 1.5 (K082200)
• Klockner Dental Implants, models SK2, NK2, S4 (K010132)
• P.004 implants including abutments and healing caps (K062129)
• NC Healing Abutments and NC Closure Screws (K071585)
• ITI synOcta (Esthetic) Meso Abutments (K033243)
• P.004 NC Anatomic Abutments (K071357)
• TiUnite implants (K050705)
• TiN Coated Implants and Abutments (K992334)
• PreFormance Temporary Cylinders (K060291)
• Abutment for Provisional Restorations (K072624)
• SPI® Customizable gingiva former (K092248)
• SPI® Variomulti Angled abutment (K101798)
• SFI-Bar® (K083876)
• SPI® Titanium Base for CADICAM (K102804)
• Lava™ Frame, Lava™ Frame Shade (K072055)

Submission Summary (Full Text)

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# 510(k) SUMMARY

| Date of submission: | 2013-04-15 | JUL 1 9 2013 |
|----------------------|------------------------------------------------------------------------------------|--------------|
| Submitter name: | SOADCO, S.L. | |
| Submitter address: | Avgda. Fiter i Rossell, 4bis - Local 2<br>ESCALDES - ENGORDANY<br>AD-700 (ANDORRA) | |
| Contact person: | Maria Mitjaneta | |
| Phone: | [phone] | |
| Fax: | [phone] | |
| e-mail: | [e-mail] | |
| Device Trade Name: | Klockner Dental Implant Abutments | |
| Common Name: | Endosseous Dental Implant Abutments | |
| Classification Name: | Endosseous Dental Implant Abutment (21 CFR 872.3630) | |
| Product code: | NHA | |

## Legally Marketed (Predicate) Device(s):

ﺮ

510(k) Submission – Klockner Abutments

Section 5 – 510(k) Summary

| 510(k) Number | Device | Manufacturer |
|---------------|---------------------------------------------------------------|--------------------|
| K080224 | Klockner Essential Dental Implant System, models: EC, ES, ECK | SOADCO |
| K082200 | Klockner Essential Dental Implant System, model: EC 1.5 | SOADCO |
| K010132 | Klockner Dental Implants, models SK2, NK2, S4 | SOADCO |
| K062129 | P.004 implants including abutments and healing caps | Straumann |
| K071585 | NC Healing Abutments and NC Closure Screws | Straumann |
| K033243 | ITI synOcta (Esthetic) Meso Abutments | Straumann |
| K071357 | P.004 NC Anatomic Abutments | Straumann |
| K050705 | TiUnite implants | Nobel Biocare |
| K992334 | TiN Coated Implants and Abutments | 3i |
| K060291 | PreFormance Temporary Cylinders | 3i |
| K072624 | Abutment for Provisional Restorations | Astra Tech |
| K092248 | SPI® Customizable gingiva former | Thommen Medical AG |
| K101798 | SPI® Variomulti Angled abutment | Thommen Medical AG |
| K083876 | SFI-Bar® | Cendres & Métaux |
| K102804 | SPI® Titanium Base for CADICAM | Thommen Medical AG |
| K072055 | Lava™ Frame, Lava™ Frame Shade | 3M ESPE AG |

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510(k) Submission - Klockner Abutments Section 5 - 510(k) Summary

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## Device Description:

Klockner Dental Implant Abutments consist of a group of prosthetic components placed into dental implants to aid in prosthetic rehabilitation. According to their function, they are classified in:

- Healing caps, are manufactured in Titanium Alloy, intended to assist in healing or modification of the adjacent tissues for internal octagonal connection system.
- Protective caps, manufactured in PMMA and Titanium Alloy intended to protect abutments when choosing direct oral impression for internal octagonal connection system.
- Temporary abutments, manufactured in Titanium cp, Titanium Alloy and Titanium cp + -PMMA, intended to support provisional prosthetic restorations for internal octagonal connection system.
- Angled abutments, manufactured in Titanium cp and Titanium Alloy, intended to retain definitive dental prosthesis. Used when it is necessary to correct the implant axis, for internal octagonal connection system and external hexagonal connection system.
- Straight abutments, manufactured in Titanium Alloy and Titanium cp, intended to retain definitive dental prosthesis for internal octagonal connection system. Includes Titanium Octacone Scan abutment, a Titanium Base for CAD/CAM. This base is suitable for precision fit custom abutments or crown and bridge restorations fabricated with CAD/CAM technology provided separately by 3M ESPE as the Lava System.
- Overdenture abutments, manufactured in Titanium Alloy and POM C, intended to retain removable dental prosthesis for internal octagonal connection system and external hexagonal connection system.

Healing caps, protective caps and temporary abutments are used for a limited time, while angled abutments, straight abutments and overdenture abutments are intended for a definitive use.

### Intended Use:

The Klockner Dental Implant Abutments are intended to be placed into dental implants to provide support for prosthetic reconstructions such as crowns, bridges or overdentures. The Klockner Dental Implant Abutments include healing caps, protective caps, temporary abutments, angled abutments, straight abutments, and overdentures. All abutments are intended to be used with the Klockner Dental Implant Systems, models: Essential ES, Essential ES, Essential ECK, Essential EC 1.5, SK2 and NK2.

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510(k) Submission – Klockner Abutmen Section 5 — 510(k) Summa

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# Summary of Comparison with Predicate Device

In the establishment of substantial equivalence, KLOCKNER dental implant abutnents are compared with other similar abulments alread
available on the market as indicated above

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| | | | | | | PREDICATED DEVICE | | | | | | Basic Design |
|---------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------|--------------------|-------------|-------------|-------------------|-----------------------------------------------------------------------------------|---------------------------------------------------------------------------------|--------------------------|--|---------------------------------|---------------------------------------------------------------------------------------------------------------------------------|
| | | | | | | | Material | Restoration | Healing/protective caps: | | | |
| abutment) | Titanium ASTM F136<br>(straight pillar<br>abutment, screws) | Overdenture<br>abutments: | Titanium ASTM F136 | TiN coating | POM C (cap) | | | Single or multiunit | Beveled design. | | Angled/straight abutments: | Octagonal angled abutment design (17° and 22°), but<br>without the occlusal thread. Also anodized abutments (blue<br>and green) |
| | | | | | | | Healing/protective caps: | Titanium (K062129,<br>K071585, K071357:<br>healing caps and<br>protective caps) | | | Similar pillar abutment design. | |
| Predicate<br>Device | Indications for Use / Intended Use | | | | | | | | | | | Standard platform. |
| K080224 | The Klockner Essential implant system is especially designed for<br>surgical insertion into the bone using additional material to<br>replace the root of the teeth, acting as the support for the dental<br>implants formed by implant accessories. | | | | | | Titanium ASTM F136<br>(K080224) | | | | | Overdenture abutments: |
| Klockner<br>Essential<br>Dental<br>Implant<br>System,<br>models: EC,<br>ES, ECK | The Essential Solid implants are fitted with an internal octagonal<br>conical connection combined with an external octagonal<br>connection measuring 1.2 mm in height. | | | | | | POM C (K080224) | | | | | Ball attachment design. |
| | The Essential Cone implants are fitted with an internal octagonal<br>conical connection. | | | | | | Temporary<br>abutments: | | | | | Abutment implant connection: screw fixation. |
| | The Essential ECK implants are fitted with a larger internal<br>octagonal conical connection than that of the Essential Cone<br>implants. | | | | | | Titanium ASTM F136<br>(K072624, K092248,<br>K060291, Implant<br>System 3i DIEMTM) | | | | | Connecting principle overdenture: retentive system. |
| | Immediate loading is appropriate for the Essential Solid,<br>Essential Cone and Essential ECK implants when good primary<br>stability is achieved with appropriate occlusal loading. | | | | | | | | | | | TiN treatment. |
| | Abutments can be used in single tooth replacements and<br>principle overdenture: retentive system. TiN treatment. | | | | | | | | | | | |

4000 Co

510(k) Submission – Klockner Abutments

K122988

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| K010132<br>Clockner<br>Dental<br>Implants,<br>models SK2,<br>NK2, S4 | multiple tooth restorations.<br>8mm Implants are not indicated for use as unitary implants and for immediate load.<br>The dental implant consist of a small conical fixture (the root-form configuration), perhaps six to eighteen millimetres in length, placed into a tiny receptacle channel which has been drilled into the bone under the gingiva (gum) at the desired location.<br>The gingiva is elevated fi-on the underlying bone, the channel is cut, the fixture is placed, and the gingiva is sutured.<br>In its simplest form, the implant is used to substituting the roots of teeth, to secure a denture. This is a wonderful remedy for an edentulous patient whose ridges do not allow the secure placement of a denture. In other uses the implant becomes the support for a single crown, sometimes two or more (sometime many) implants are used to support a bridge or multiple bridge. | PEEK (K060291,<br>Implant System 3i<br>DIEMTM)<br>PMMA (K092248)<br>Angled and straight<br>abutments:<br>Titanium ASTM F67<br>(K080224, K033243,<br>K062129, K101798,<br>K102804: octagonal<br>angled abutments,<br>straight octacone scan<br>abutment)<br>Titanium (K050705:<br>hexagonal angled<br>abutment) | Single or multi-<br>unit | Overdenture abutments:<br>Ball attachment design.<br>Abutment implant connection: screw fixation.<br>Connecting principle overdenture: retentive system.<br>TiN treatment. |
|-------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| K062129<br>P.004<br>implants<br>including<br>abutments<br>and healing<br>caps | The P.004 implants are intended for immediate, delayed or conventional placement in the maxilla and/or mandibular arches to support crowns, bridges or overdentures in edentulous or partially edentulous patients.<br>They are intended for immediate function on single-tooth and/or multiple tooth applications when good primary stability is achieved and with appropriate occlusal loading, to restore chewing function. Multiple tooth applications may be rigidly splinted. In the case of edentulous patients, 4 or more implants must be used.<br>Abutments are intended to be placed into dental implants to provide support for prosthetic reconstructions such as crowns or bridges. Meso abutments are indicated for cemented restorations particularly in esthetic areas of the mouth. The abutment can be used in single tooth replacements and multiple | Titanium ASTM F136<br>(K080224: straight<br>pillar abutment,<br>screws)<br>Overdentures<br>abutments:<br>Titanium ASTM F136<br>(K010132, K080224,<br>K083876)<br>Titanium (K033243)<br>TiN coating (K010132,<br>K080224, K992334)<br>POM C (K010132,<br>K080224) | Single or multi-<br>unit | Healing/protective caps:<br>Conical emergence profile.<br>Angled abutments:<br>Angled abutment design.<br>Standard platform. |

SOLD

510(k) Submission — Klockner Abutments

Section 5 — 510(k) Summar

5/10

K122988

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510(k) Submission – Klockner Abutment Section 5 – 510(k) Summar

| tooth restorations. | .004 Healing abutments and Closure Screws are intended for<br>use with the Straumann P.004 Bone Level Implant system to<br>protect the inner configuration of the implant. Healing abutments<br>give a secondary function to maintain, stabilize and form the soft<br>tissue during the healing process. |
|---------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| | abutments are intended to be placed into dental implants to<br>provide support for prosthetic reconstructions such as crowns or<br>bridges. The ITI synOcta Meso Abutments are indicated for<br>cemented restorations in esthetic areas of the mouth. The<br>abutment can be used in single-tooth replacements and multiple-<br>tooth restorations. |
| | abutments are intended to be placed into dental implants to<br>provide support for prosthetic reconstructions such as crowns,<br>bridges and overdentures.<br><br>abutments can be used in single tooth replacements and<br>multiple tooth restorations. |
| | Nobel Biocare TiUnite Implants are root-form endosseous<br>implants intended to be surgically placed in the bone of the<br>upper or lower jaw arches to provide support for prosthetic<br>devices, such as an artificial tooth, in order to restore patient<br>esthetics and chewing function. Nobel Biocare TiUnite Implants<br>are indicated for single or multiple unit restorations in splinted or<br>non-splinted applications. Nobel Biocare TiUnite Implants may<br>be placed immediately and put into immediate function providing |

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| | Healing/protective caps: | |
|----------------------|--------------------------------------------------------------------------------------------------------------|--|
| N/A | Conical emergence profile | |
| | Angled/straight abutments: | |
| Single or multi-unit | Octagonal angled abutment design (15° and 20°).<br>Titanium Base (for CAD/CAM) design.<br>Standard platform. | |
| | Overdenture abutments: | |
| | Ball attachment design.<br>Connecting principle overdenture: retentive system. | |
| | Healing/protective caps: | |
| Single or multi-unit | Beveled design. | |
| | Angled abutments: | |
| Single or multi-unit | Angled hexagonal design.<br>Standard platform. | |

/

K122988

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| 510(k) Submission - Klockner Abutments | Section 5 - 510(k) Summary |
|----------------------------------------|----------------------------|
|----------------------------------------|----------------------------|

| | | Single or multi-unit | Single or multi-unit | Single or multi-unit | Single or multi-unit |
|--------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------|---------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------|
| | | Overdenture abutments:<br>TiN treatment | Temporary abutments:<br>Acrylic-based polymer with a titanium base. | Temporary abutments:<br>External retentions to promote the union of acrylic material with the abutment.<br>Conical connection to enable insertion of multiple structures. | Angled abutments:<br>Angled abutments design (17°, 22° and 30°). |
| K992334<br>TiN Coated implants and Abutments | that the initial stability requirements detailed in the surgical manuals are satisfied.<br>TiUnite implants are indicated for use in soft bone whenever immediate or early loading is applied. The TiUnite implants are preferred in these soft bone indications because bone formation is more rapid and greater than on machined surface implants resulting in better maintenance of initial implant stability, faster and stronger osseointegration and higher success rates.<br>Endosseous implants and abutments are indicated for surgical placement into the upper and lower jaw arches as permanent support for prosthetic appliances to restore a patient's masticatory function. Proposed Titanium Nitride ("TiN") coating applied to implants / abutments improves the overall esthetics of the completed restoration. | | | | |
| K060291<br>3i PreFormance Temporary Cylinders | The PreFormance Temporary Cylinders are intended for use as an accessory to endosseous dental implants to support a prosthetic device in a partially or fully edentulous patient. They are intended for use to support single and multiple unit prostheses in the mandible or maxilla for up to 180 days during endosseous and gingival healing, and are for non occlusal loading of single and multiple unit provisional restorations. The prostheses can be screw or cement retained to the abutment. | | | | |
| K072624<br>Astra Tech Abutments for Provisional Restorations | Astra Tech Implant System abutments are intended to be used in conjunction with Astra Tech Implant System implants in fully edentulous or partially edentulous maxillary and/or mandibular arches to provide support for crowns, bridges or overdentures. | | | | |
| K101798<br>Thommen SPI® VARIOmulti | Thommen SPI® VARIOmulti Angled Abutments are intended to be used in conjunction with SPI® System dental implants in the maxillary and/or mandibular arch to provide support for splinted | | | | |

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(k) Submission – Klockner Abutr 510(k) Sum

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| | Section 5 - 510(k) Summary | | | |
|------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------|
| Angled<br>Abutment | crowns, bridges or overdentures. | Single or multi-<br>unit | Multi-unit | Single or multi-<br>unit |
| K092248<br>SPI®<br>Customizable<br>Gingiva<br>Former | The SPI® Customizable Gingiva Former is intended to be used<br>in conjunction with SPI® System dental implants to provide<br>temporary support for crowns or bridges in the maxillary and/or<br>mandibular arch. | Temporary abutments:<br>Acrylic-based polymer with a titanium base. | Overdenture abutments:<br>Abutment implant connection: screw fixation.<br>Connecting principle overdenture: retentive system. | Straight abutments:<br>Titanium Base (for CAD/CAM) design. |
| K083876<br>SFI-Bar®<br>abutment | The SF1-Bar® is intended to be used with the SPI Element<br>Platform 4.0 mm implant (K070007) to provide support for<br>fixation of overdentures. | Standard platform and conical connection to enable<br>insertion of multiple structures. | | |
| K102804<br>SPI®<br>Titanium<br>Base for<br>CAD/CAM | Thommen Titanium Base for CAD/CAM abutments are intended<br>to be used in conjunction with Thommen implants and the 3M<br>ESPE Lava™ System in the maxillary and/or mandibular arch to<br>provide support for crowns and bridges. | Standard platform. | | |

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edific references included in the proposed device share indications for use, basic design, operating principles, material and packagi with other specific predicate device

# ummary Discussion of Non-Clinical Data

1737-2 and the applicable requirements taking account of their intended use. A sterlization according ISO 17665-1 was carie NER dental implant abutments have been subject to bioburden and sterility testing in accordance with ISO 11737-1

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510(k) Submission — Klockner Abutmen Section 5 — 510(k) Summa

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K122988

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510(k) Submission - Klockner Abutments Section 5 - 510(k) Summary

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## Summary Discussion of Clinical Data:

No clinical data are presented in this submission.

## Conclusions:

We believe the intended use, the indications for use, the mode of operation and performance characteristics of the KLOCKNER Dental Implant Abutments are equivalent to the indicated predicate devices. The results of bench testing confirm acceptable device performance as per its intended use. Therefore we believe substantial equivalence of the KLOCKNER Dental Implant Abutments to the predicate devices may be established.

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Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G60 Silver Spring, MD 20993-0002

July 19, 2013

Ms. Maria Mitjaneta Quality Manager Soadco, S.L. Avgda. Fiter i Rossell, 4bis -Local 2 Escaldes - Engordany Andorra AD-700

Re: K122988

Trade/Device Name: KLOCKNER Dental Implant Abutments Regulation Number: 21 CFR 872.3630 Regulation Name: Endosseous Dental Implant Abutment Regulatory Class: II Product Code: NHA Dated: July 5, 2013 Received: July 12, 2013

Dear Ms. Mitjaneta:

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 cither 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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Page 2 - Ms. Mitjaneta

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 (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 Small Manufacturers. International and Consumer Assistance at its tollfree number [phone] or [phone] or at its Internet address

http://www.fda.gov/Medica!Devices/ResourcesforYou/Industry/default.htm. Also, please note the regulation entitled. "Misbranding by reference to premarket notification" (21CFR 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 Small Manufacturers, International and Consumer Assistance at its toll-free number [phone] or [phone] or at its Internet address

http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm.

Sincerely yours.

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Kwame Ulmer, M.S. Acting Division Director Division of Anesthesiology, General Hospital, Respiratory, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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510(k) Submission - Klockner Abulments Section 4 - Indications for Use Statement

## INDICATIONS FOR USE

K122988 510(k) Number (if known):

Device Name: KLOCKNER Dental Implant Abutments

Indications for Use:

The Klockner Dental Implant Abutments are intended to be placed into dental implants to provide support for prosthetic reconstructions such as crowns, bridges or overdentures. The Klockner Dental Implant Abutments include healing caps, temporary abutments, angled abutments, straight abutments, and overdentures. All abulments are intended to be used with the Klockner Dental Implant Systems, models: Essential EC, Essential ECK, Essential ECK, Essential EC 1.5, SK2 and NK2.

Prescription Use (Part 21 CFR 801 Subpart D) AND / OR

Over-The-Counter Use (21 CFR 801 Subpart C)

(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

Andrew I. Steen 2013.07.19 09:13:57 -04'00

(Division Sign-Off) (Division Sign-Off)
Division of Anesthesiology, General Hospital
Division of Anesthesiology, General Devices Division of Anostinochoological

510(k) Number:_