510(k) K802104

C-SPLINT by Cutter Laboratories, Inc. — Product Code IQI

K802104 is an FDA 510(k) premarket notification submitted by Cutter Laboratories, Inc. for the device "C-SPLINT". The FDA issued a decision of Substantially Equivalent on September 16, 1980. The device falls under product code IQI (Orthosis, Limb Brace), a Class I device regulated under 21 CFR 890.3475. Cutter Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 16, 1980
Date Received
September 3, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Orthosis, Limb Brace
Device Class
Class I
Regulation Number
890.3475
Review Panel
PM
Submission Type