510(k) K900475

DISTRAC(TM) TABLE by Lossing Orthopedic, Inc. — Product Code ITH

K900475 is an FDA 510(k) premarket notification submitted by Lossing Orthopedic, Inc. for the device "DISTRAC(TM) TABLE". The FDA issued a decision of Substantially Equivalent on May 24, 1990. The device falls under product code ITH (Equipment, Traction, Powered), a Class II device regulated under 21 CFR 890.5900. Lossing Orthopedic, Inc. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 24, 1990
Date Received
February 1, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Equipment, Traction, Powered
Device Class
Class II
Regulation Number
890.5900
Review Panel
PM
Submission Type