Product code JEB— General, Plastic Surgery

FDA has cleared 13 devices under product code JEB between 1977 and 1991, 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.

• 19911 clearance
• 19901 clearance
• 19892 clearances
• 19882 clearances
• 19874 clearances
• 19782 clearances
• 19771 clearance

• Stierlen-Maquet AG4 clearances
• Orthopedic Systems, Inc.2 clearances
• Scholten Surgical Instruments, Inc.1 clearance
• Orthopedic Equipment Co., Inc.1 clearance
• Ortho-J, Inc.1 clearance
• Mtd, Inc.1 clearance
• Instrumentation Specialties, Inc.1 clearance
• Arthro-Medic, Inc.1 clearance
• American Sterilizer Co.1 clearance

• K905816 — ORTHOVISION TABLEAmerican Sterilizer Co.·1991-03-06
• K900405 — SCHOLTEN FRAMEScholten Surgical Instruments, Inc.·1990-03-01
• K891917 — ORTHO-J, INC. BEK-JS-004Ortho-J, Inc.·1989-05-26
• K891387 — WILLIAMS BELT & BOOTArthro-Medic, Inc.·1989-05-23
• K881101 — K ORTHOPEDIC TABLEInstrumentation Specialties, Inc.·1988-04-06
• K880263 — OSI RIZZOLI ORTHOPEDIC TABLE/MANUAL VERSIONOrthopedic Systems, Inc.·1988-03-15
• K873273 — ORTHOPAEDIC TABLE 1420Stierlen-Maquet AG·1987-09-17
• K873274 — PLASTER TABLE 1418Stierlen-Maquet AG·1987-09-17
• K873275 — EXTENSION TABLE 1417Stierlen-Maquet AG·1987-09-17
• K873276 — EXTENSION DEVICE 1416Stierlen-Maquet AG·1987-09-17
• K781082 — CAST BLOCKOrthopedic Equipment Co., Inc.·1978-07-07
• K772321 — ARTHROSTRESSMtd, Inc.·1978-01-03
• K771020 — SPINAL SURGERY FRAMEOrthopedic Systems, Inc.·1977-06-17