510(k) K870102

TUPPER TROLLEY by Orthopedic Systems, Inc. — Product Code HST

K870102 is an FDA 510(k) premarket notification submitted by Orthopedic Systems, Inc. for the device "TUPPER TROLLEY". The FDA issued a decision of Substantially Equivalent on February 3, 1987. The device falls under product code HST (Apparatus, Traction, Non-Powered), a Class I device regulated under 21 CFR 888.5850. Orthopedic Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 3, 1987
Date Received
January 9, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Apparatus, Traction, Non-Powered
Device Class
Class I
Regulation Number
888.5850
Review Panel
NE
Submission Type