510(k) K862584

OSTEOTOMY DRAINAGE TUBE by Treace Medical, Inc. — Product Code GBS

K862584 is an FDA 510(k) premarket notification submitted by Treace Medical, Inc. for the device "OSTEOTOMY DRAINAGE TUBE". The FDA issued a decision of Substantially Equivalent on August 12, 1986. The device falls under product code GBS (Catheter, Ventricular, General & Plastic Surgery), a Class I device regulated under 21 CFR 878.4200. Treace Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 12, 1986
Date Received
July 7, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Ventricular, General & Plastic Surgery
Device Class
Class I
Regulation Number
878.4200
Review Panel
SU
Submission Type