Product code ITQ— Physical Medicine

FDA has cleared 15 devices under product code ITQ between 1977 and 1983, filed by 9 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

• 19832 clearances
• 19823 clearances
• 19814 clearances
• 19801 clearance
• 19781 clearance
• 19774 clearances

• Med Fusion Systems, Inc.4 clearances
• Warm & Form, Orthopedic Materials2 clearances
• Surgical Appliance Industries, Inc.2 clearances
• Orthopedic Systems, Inc.2 clearances
• Omni Scientific, Inc.1 clearance
• Medical Design & Manufacturing Corp.1 clearance
• Innovation Sports, Inc.1 clearance
• Hosmer Dorrance Corp.1 clearance
• Aircast, Inc.1 clearance

• K831044 — LIMITED MOTION FUNCTIONAL KNEE BRACEOrthopedic Systems, Inc.·1983-06-24
• K831310 — BRACE C.T.Innovation Sports, Inc.·1983-05-16
• K823658 — DELUXE KNEE IMMOBILIZER(UNIVERSAL)Warm & Form, Orthopedic Materials·1982-12-30
• K823397 — ANATOMIC FRACTURE BRACEOrthopedic Systems, Inc.·1982-11-29
• K823159 — DELUXE KNEE IMMOBILIZERWarm & Form, Orthopedic Materials·1982-11-10
• K812423 — NEOPRENE KNEE SUPPORTSurgical Appliance Industries, Inc.·1981-09-14
• K812094 — AIRCAST PNEUMATIC KNEE BRACEAircast, Inc.·1981-08-13
• K811689 — CYLINDER KNEE CAST/SPLINTSurgical Appliance Industries, Inc.·1981-06-25
• K810222 — LIMB ORHTOSISMedical Design & Manufacturing Corp.·1981-02-04
• K802673 — KNEE BRACE/STABILIZEROmni Scientific, Inc.·1980-11-12
• K780892 — FRACTURE BRACINGHosmer Dorrance Corp.·1978-06-13
• K772268 — DEMI-WALKER (REGULAR)Med Fusion Systems, Inc.·1977-12-20
• K772269 — SETUP WALKER ADJUSTABLEMed Fusion Systems, Inc.·1977-12-20
• K772270 — SETUP WALKER OVER TOILET CONSTRUC.Med Fusion Systems, Inc.·1977-12-20
• K772271 — WALKER FOLDING ADJUSTABLEMed Fusion Systems, Inc.·1977-12-20