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FDA 510(k), K072208, MAYFIELD DISPOSABLE AND REUSABLE TITANIUM SKULL PINS
FDA 510(k), K072208, MAYFIELD DISPOSABLE AND REUSABLE TITANIUM SKULL PINS
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510(K) Number: K072208
Device Name: MAYFIELD DISPOSABLE AND REUSABLE TITANIUM SKULL PINS
Manufacturer: INTEGRA LIFESCIENCES CORPORATION
Device Classification Name: holder, head, neurosurgical (skull clamp)
Regulation Number: 882.4460
Classification Product Code: HBL
Date Received: 08/08/2007
Decision Date: 09/07/2007
Regulation Medical Specialty: Neurology
Device Name: MAYFIELD DISPOSABLE AND REUSABLE TITANIUM SKULL PINS
Manufacturer: INTEGRA LIFESCIENCES CORPORATION
Device Classification Name: holder, head, neurosurgical (skull clamp)
Regulation Number: 882.4460
Classification Product Code: HBL
Date Received: 08/08/2007
Decision Date: 09/07/2007
Regulation Medical Specialty: Neurology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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