510(k) K811494
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