510(k) K051440

MAYFIELD INFINITY SKULL CLAMP by Integra Lifesciences Corp. — Product Code HBL

K051440 is an FDA 510(k) premarket notification submitted by Integra Lifesciences Corp. for the device "MAYFIELD INFINITY SKULL CLAMP". The FDA issued a decision of Substantially Equivalent on September 20, 2005. The device falls under product code HBL (Holder, Head, Neurosurgical (Skull Clamp)), a Class II device regulated under 21 CFR 882.4460. Integra Lifesciences Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 20, 2005
Date Received
June 2, 2005
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Holder, Head, Neurosurgical (Skull Clamp)
Device Class
Class II
Regulation Number
882.4460
Review Panel
NE
Submission Type