TIADAPT ABUTMENT SYSTEM
Device Facts
| Record ID | K971706 |
|---|---|
| Device Name | TIADAPT ABUTMENT SYSTEM |
| Applicant | Nobel Biocare Uas, Inc. |
| Product Code | NHA · Dental |
| Decision Date | Jul 21, 1997 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 872.3630 |
| Device Class | Class 2 |
| Attributes | Therapeutic |
Indications for Use
Nobel Biocare's TiAdapt™ Abutment System is a set of screw retained preparable abutments that are secured to an endosseous implant and are intended to function as an anchor to which prosthetic devices, such as artificial teeth, may be attached using dental cement to restore a patient's chewing function.
Device Story
TiAdapt Abutment System consists of preparable titanium abutments, abutment screws, counter torque devices, adaptors, screwdrivers, temporary cylinders, and impression copings. System secures to Brånemark System dental implants via gold abutment screw. Functions as anchor for cemented single crowns or multi-unit bridges. Used by dental professionals in clinical settings to restore patient chewing function. Components facilitate prosthetic attachment to endosseous implants.
Clinical Evidence
No clinical data provided; bench testing only.
Technological Characteristics
System components constructed of titanium. Includes preparable abutments, gold abutment screws, counter torque devices, and manual screwdrivers. Designed for use with Brånemark System endosseous dental implants. Mechanical fixation via screw-retained connection. No software or electronic components.
Indications for Use
Indicated for patients requiring dental restoration via endosseous implants to restore chewing function; used as an anchor for cemented prosthetic devices such as artificial teeth.
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
- CeraOne Abutments (K910611)
- Ceramic Abutment (K913255)
- CeraOne Abutment Screw (K961737)
- Guide Pin (K911969)
- Abutment Lab-Screw (K925769)
- CerAdapt
- Machine Counter Torque Device (K953775)
- Estheticone Temporary Cylinder (K925766)
- Miruscone Temporary Cylinder (K962403)
- Temporary Tube (K926766)
- Titanium Impression Coping (K952448)
- Plastic Impression Coping (K910611)
- CeraOne Screwdrivers (K922805)
- Fixture Guide Set Tray (K944963)
Submission Summary (Full Text)
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JUL 21 1997
Pre-market Notification Page -3-�������������������������������
### 510(k) Summary of Safety and Effectiveness VII.
### A. Name and Address
This Summary of Safety and Effectiveness is being submitted by Nobel Biocare USA, Inc., 777 Oakmont Lane, Suite 100, Westmont, IL 60559. The telephone number is: (630) 654-9100, extension 2002, and the contact person will be Betsy Brown, the Vice President, Regulatory Affairs.
# B. Name of the Device
This device system consists of various preparable titanium abutments, abutment screws, a counter torque device with handle, adaptors, machine Uni-grip screwdrivers with autoclavable box, temporary cylinders, temporary tubes, laboratory screws and impression copings.
## C. The Predicate Product
The predicate products used in this Pre-market Notification are similar components marketed by Nobel Biocare including the CeraOne Abutments (K910611), Ceramic Abutment (K913255), CeraOne™ Abutment Screw (K961737), Guide Pin (K911969), Abutment Lab-Screw (K925769), CerAdapt™, Machine Counter Torque Device (K953775), Estheticone™ Temporary Cylinder (K925766), Miruscone Temporary Cylinder (K962403), Temporary Tube (K926766), Titanium Impression Coping (K952448), Plastic Impression Coping (K910611), CeraOne™ Screwdrivers (K922805) and Fixture Guide Set Tray (K944963).
# D. Description of Device
The Nobel Biocare TiAdapt™ Abutment System is comprised of preparable titanium abutments which are secured to the Brånemark System® dental implants with a gold abutment screw. This system functions as an anchor to which a single crown can be cemented. When more than one preparable abutment is used, a multi-unit bridge can be cemented to the abutments. The TiAdapt Abutment System also includes a counter torque device and adaptors, temporary cylinders, impression copings and machine Uni-grip screwdrivers.
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Pre-market Notification Page -4-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
E. Intended Use of the Device
Nobel Biocare's TiAdapt™ Abutment System is a set of screw retained preparable abutments that are secured to an endosseous implant and are intended to function as an anchor to which prosthetic devices, such as artificial teeth, may be attached using dental cement to restore a patient's chewing function.
F. Comparison of Technological Characteristics
The technological characteristics between the components of the TiAdapt Abutment System and the corresponding predicate products found in the Brånemark System® are identical.
### Summary Of Safety And Effectiveness Concerns
Safety and effectiveness problems that have been encountered with similar Abutment Systems used with endosseous implants that are currently being marketed include:
- 1. occasional fractures of the screw attaching the abutment to the fixtures usually due to functional overload from masticastory forces:
- 2. screws working loose (usually because torque force below recommended values was applied when the abutment was attached to the fixture) may lead to the formation of granulation tissue at the level of the fixture and abutment connection which may, in turn, result in infection:
- 3. improper initial seating of abutments resulting in gingival inflammation and fistulae formation, both conditions resolve when proper seating of the abutment is accomplished.
- 4. occasional fracture of the abutment screw which is usually caused by poorly designed and/or fabricated restorations that creates overloads or cause's metal fatigue.
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Public Health Service
Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002
SEP 1 7 2010
Ms. Phuong Nguyen Regulatory Affairs Manager Nobel Biocare USA LLC 22715 Savi Ranch Parkway Yorba Lind, California 92887
Re: K971706
Trade/Device Name: TiAdapt Abutment System Regulation Number: 21 CFR 872.3630 Regulation Name: Endosseous Dental Implant Abutment Regulatory Class: II Product Code: NHA Dated: July 28, 2010 Received: July 29, 2010
Dear Mr. Nguyen:
This letter corrects our substantially equivalent letter of July 29, 2010.
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 (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.
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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Page 2- Ms. Nguyen
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 device-related 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 go to
http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. 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 (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.
Sincerely yours,
Supa Viner
Anthony D. Watson, B.S., M.S., M.B.A.
Director
Division of Anesthesiology, General Hospital,
Infection Control and Dental Devices
Office of Device Evaluation
Center for Devices and
Radiological Health
Enclosure
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510(k) Number (if known):_____________________________________________________________________________________________________________________________________________________
Device Name: TiAdapt™ Abutment System_
Indications For Use:
Nobel Biocare's TiAdapt Abutment System is a set of screw retained preparable abutments which are secured to an endosseous implant and is intended to function as an anchor to which prosthetic devices, such as artificial teeth, may be attached using dental cement to restore a patient's chewing function.
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED
Concurrence of CDRH, Office of Device Evaluation (ODE)
| (Division Sign-Off) | Field W. Shippen |
|----------------------------------------|------------------|
| Division of Dental, Infection Control, | |
| and General Hospital Devices | |
| 510(k) Number | K971706 |
Prescription Use. (Per 21 CFR 801.109)
OR
Over-The-Counter Use_
(Optional Format 1-2-96)
