510(k) K811494

LUMBO-SACRAL FLEXION ORTHOSIS by Surgical Appliance Industries, Inc. — Product Code IPY

K811494 is an FDA 510(k) premarket notification submitted by Surgical Appliance Industries, Inc. for the device "LUMBO-SACRAL FLEXION ORTHOSIS". The FDA issued a decision of Substantially Equivalent on June 16, 1981. The device falls under product code IPY (Orthosis, Lumbo-Sacral), a Class I device regulated under 21 CFR 890.3490. Surgical Appliance Industries, Inc. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 16, 1981
Date Received
May 27, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Orthosis, Lumbo-Sacral
Device Class
Class I
Regulation Number
890.3490
Review Panel
PM
Submission Type