PODIATRIC MATERIAL

K940132 · Crown Delta Corp. · MNE · Sep 29, 1994 · Physical Medicine

Device Facts

Record IDK940132
Device NamePODIATRIC MATERIAL
ApplicantCrown Delta Corp.
Product CodeMNE · Physical Medicine
Decision DateSep 29, 1994
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 890.3475
Device ClassClass 1

Device Story

Podiatric Multi-Sil II Moldable Silicone Putty is a limb orthosis used in podiatric applications. The device consists of a moldable silicone material intended for use as an orthotic aid. It is applied by clinicians to provide support or cushioning for the foot. The device functions as a physical orthotic intervention to assist in patient comfort or alignment.

Technological Characteristics

Moldable silicone putty; limb orthosis; classified under 21 CFR 890.3475; Class I exempt.

Regulatory Classification

Identification

A limb orthosis (brace) is a device intended for medical purposes that is worn on the upper or lower extremities to support, to correct, or to prevent deformities or to align body structures for functional improvement. Examples of limb orthoses include the following: A whole limb and joint brace, a hand splint, an elastic stocking, a knee cage, and a corrective shoe.

Submission Summary (Full Text)

{0} [LOGO] DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 Mr. Laurence Colin President Crown Delta Corporation 1550 Front Street Yorktown Heights, New York 10598 MAY 2 4 2004 Re: K940132 Trade Name: Podiatric Multi-Sil II Moldable Silicone Putty Classification Regulation Name and Number: Limb Orthosis 21 CFR 890.3475 Regulatory Class: Class I Exempt Product Code: MNE Dated: March 9, 1994 Received: March 15, 1994 Dear Mr. Colin: This letter corrects our substantially equivalent letter of September 29, 1994 regarding the classification of your device. We have reviewed your premarket notification submission and have found this device to be exempt from the premarket notification requirements of the Federal Food, Drug, and Cosmetic Act (Act). Therefore, you may immediately begin marketing this device as described in your premarket notification. The final classification regulation for your device appears in Title 21 of the Code of Federal Regulations (CFR) 890.3475. We suggest that you review this regulation since it may grant other exemptions from certain general controls of the Act. Your device classification regulation name, regulatory class, and product code are shown above. When listing your device with the Food and Drug Administration, please use this product code. In the future, new but substantially equivalent devices which fall within the above classification regulation name and meet the classification criteria may be marketed without sending a premarket notification submission to the Food and Drug Administration. We suggest, however, that you review 21 CFR Section 890.9 to determine whether or not your new device (s) meets the limitations of exemption from Section 510(k) of the Act. {1} Page 2 - Mr. Laurence Colin If you have any questions regarding this letter, please contact CAPT Marie A. Schroeder, at (301) 594-1296 or the Division of Small Manufacturers, International and Consumer Assistance at its toll free number (800) 638-2041 or (301) 442-6597, or at its Internet address "http://www.fda.gov/cdrh/dsmamain.html". Sincerely yours, Celia M. Witten, Ph.D., M.D. Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health
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