Product code LWG— General, Plastic Surgery

FDA has cleared 4 devices under product code LWG between 1987 and 1988, filed by 3 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.

• 19882 clearances
• 19872 clearances

• Avec Scientific Design Corp.2 clearances
• Karlin Technology, Inc.1 clearance
• Cedar Surgical, Inc.1 clearance

• K883295 — CHOP SPINE FRAMEAvec Scientific Design Corp.·1988-08-23
• K882520 — SHOULDER BOLSTER, KNEE, ANKLE & LEG SUPPORT PADSKarlin Technology, Inc.·1988-07-18
• K874494 — KAMBIN LAMINECTOMY FRAMEAvec Scientific Design Corp.·1987-11-23
• K873690 — CEDAR(TM) PELVIC CUSHIONCedar Surgical, Inc.·1987-10-26