Product code FWY— General, Plastic Surgery

FDA has cleared 4 devices under product code FWY between 1980 and 1988, filed by 4 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.

• 19881 clearance
• 19871 clearance
• 19831 clearance
• 19801 clearance

• Warner-Lambert Co.1 clearance
• Stryker Corp.1 clearance
• Skytron, Div. the Kmw Group, Inc.1 clearance
• Orthopedic Systems, Inc.1 clearance

• K883457 — ASST-3000 SPINAL SURGERY TABLEOrthopedic Systems, Inc.·1988-08-26
• K873478 — SKYTRON MODEL 130 SURGICAL TABLESkytron, Div. the Kmw Group, Inc.·1987-09-24
• K833509 — CHEMONUCLEOLYSIS TABLEStryker Corp.·1983-11-28
• K800118 — CHICK SURGICAL TABLEWarner-Lambert Co.·1980-02-05