510(k) K760841

HEXCELITE SHEET SPLINTS by Hexcel Medical — Product Code ITG

K760841 is an FDA 510(k) premarket notification submitted by Hexcel Medical for the device "HEXCELITE SHEET SPLINTS". The FDA issued a decision of Substantially Equivalent on November 1, 1976. The device falls under product code ITG (Bandage, Cast), a Class I device regulated under 21 CFR 890.3025. Hexcel Medical has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 1, 1976
Date Received
October 13, 1976
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bandage, Cast
Device Class
Class I
Regulation Number
890.3025
Review Panel
PM
Submission Type