510(k) K781761

KENDRICK EXTRICATION DEVICE by Medi-Ked, Inc. — Product Code IQF

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 27, 1978
Date Received
October 16, 1978
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Orthosis, Cervical-Thoracic, Rigid
Device Class
Class I
Regulation Number
890.3490
Review Panel
PM
Submission Type