510(k) K103558

SYNTHES SCOUT VESSEL GUARD by Synthes Spine — Product Code OMR

K103558 is an FDA 510(k) premarket notification submitted by Synthes Spine for the device "SYNTHES SCOUT VESSEL GUARD". The FDA issued a decision of SESU on February 18, 2011. The device falls under product code OMR (Vessel Guard Or Cover), a Class II device regulated under 21 CFR 870.3470. Synthes Spine has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESU ()
Decision Date
February 18, 2011
Date Received
December 2, 2010
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Vessel Guard Or Cover
Device Class
Class II
Regulation Number
870.3470
Review Panel
CV
Submission Type

These device types do not include devices whose primary purpose is to minimize the incidence or severity of adhesion formation as a result of vascular surgery. Intended to protect vessels from injury during surgery (not to be confused with wraps, patches or covers intended to facilitate revision surgeries). Indicated to wrap, patch, or cover intended to cover blood vessels.