PROVI CEMENT

{0}------------------------------------------------ Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo features the department's name encircling a stylized symbol. The symbol is a graphic representation of a human form, with three curved lines suggesting a person's head, body, and legs. The logo is in black and white. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 JUN 2 1668 Dr. Jurgen Engelbrecht S&C Polymer GmbH Offenauer Weq 19 S-25335 Bokholt-Hanredder DEUTSCHLAND Re : K973201 Trade Name: Provi Cement Requlatory Class: II Product Code: EMA May 20, 1998 Dated: Received: May 26, 1998 ## Dear Dr. Engelbrecht: We have reviewed your Section 510(k) notification of intent to market the device referenced above and we 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). 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 (Premarket Approval), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Requlations, Title 21, Parts 800 to 895: Asubstantially equivalent determination assumes compliance with the Current Good Manufacturing Practice requirements, as set forth in the Quality System Regulation (QS) for Medical General regulation (21 CFR Part 820) and that, Devices: through periodic QS inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory In addition, FDA may publish further announcements action. concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 {1}------------------------------------------------ Page 2 - Dr. Engelbrecht through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or requlations. This letter will allow you to begin marketing your device as described in your 510 (k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4692. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification"(21CFR 807.97). " Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its internet address "http://www.fda.gov/cdrh/dsma/dsmamaip.html". Sincerely yours, Timothy A. Ulatowski Director Division of Dental, Infection Control, and General Hospital Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ K973201 : | 510(k) Number (if known): | k973201 | Page | of | |---------------------------|------------------------------------------|------|----| | Device Name: | PROVI CEMENT | | | | Indications For Use: | TEMPORARY CEMENT<br>FOR DENTAL USE ONLY. | | | S & C Polymer Silicon- und Composite Spezialitäten GmbH Offenauer Weg 19 D-25335 Bokholt-Hanredder Telefon 04121 / 86 19 Telefax 04121 / 8 72 21 (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) | Concurrence of CDRH, Office of Device Evaluation (ODE) | | |--------------------------------------------------------|--| |--------------------------------------------------------|--| | | (Division Sign-Off) | |---------------|---------------------------------------------------------------------| | | Division of Dental, Infection Control, and General Hospital Devices | | 510(k) Number | k973201 | | Prescription Use<br>(Per 21 CFR 801.109) | OR | Over-The-Counter Use | |------------------------------------------|----|--------------------------| | | | (Optional Format 1-2-96) | ach and the compress the liberty of the world in the start and states and interest sections with and sections of ് അവലംബം ........