510(k) K041611

SYNTHES (USA) RAPID RESORBABLE CRANIAL CLAMP by Synthes (Usa) — Product Code GXR

K041611 is an FDA 510(k) premarket notification submitted by Synthes (Usa) for the device "SYNTHES (USA) RAPID RESORBABLE CRANIAL CLAMP". The FDA issued a decision of Substantially Equivalent on September 8, 2004. The device falls under product code GXR (Cover, Burr Hole), a Class II device regulated under 21 CFR 882.5250. Synthes (Usa) has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 8, 2004
Date Received
June 15, 2004
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cover, Burr Hole
Device Class
Class II
Regulation Number
882.5250
Review Panel
NE
Submission Type