510(k) K951717

MED-TEC KNEE CRUTCH by Medtec, Inc. — Product Code IYE

K951717 is an FDA 510(k) premarket notification submitted by Medtec, Inc. for the device "MED-TEC KNEE CRUTCH". The FDA issued a decision of Substantially Equivalent on June 28, 1995. The device falls under product code IYE (Accelerator, Linear, Medical), a Class II device regulated under 21 CFR 892.5050. Medtec, Inc. has at least 10 other 510(k) clearances on record.