510(k) K871296

T.E.D.(TM) TRACTION DEVICE by The Kendal Co. — Product Code KQZ

K871296 is an FDA 510(k) premarket notification submitted by The Kendal Co. for the device "T.E.D.(TM) TRACTION DEVICE". The FDA issued a decision of Substantially Equivalent on April 15, 1987. The device falls under product code KQZ (Component, Traction, Non-Invasive), a Class I device regulated under 21 CFR 888.5890. The Kendal Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 15, 1987
Date Received
March 31, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Component, Traction, Non-Invasive
Device Class
Class I
Regulation Number
888.5890
Review Panel
OR
Submission Type