510(k) K781448

HARRINGTON HOOK CLAMP by Orthopedic Equipment Co., Inc. — Product Code GEN

K781448 is an FDA 510(k) premarket notification submitted by Orthopedic Equipment Co., Inc. for the device "HARRINGTON HOOK CLAMP". The FDA issued a decision of Substantially Equivalent on September 27, 1978. The device falls under product code GEN (Forceps, General & Plastic Surgery), a Class I device regulated under 21 CFR 878.4800. Orthopedic Equipment Co., Inc. has at least 10 other 510(k) clearances on record.