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Title 21 Part 882 → Subpart F → §882.5950

Title 21 → Chapter I → Subchapter H → Part 882 → Subpart F → §882.5950

Electronic Code of Federal Regulations e-CFR

Title 21 Part 882 → Subpart F → §882.5950

e-CFR data is current as of January 27, 2020

Title 21Chapter ISubchapter HPart 882Subpart F → §882.5950


Title 21: Food and Drugs
PART 882—NEUROLOGICAL DEVICES
Subpart F—Neurological Therapeutic Devices


§882.5950   Neurovascular embolization device.

(a) Identification. A neurovascular embolization device is an intravascular implant intended to permanently occlude blood flow to cerebral aneurysms and cerebral ateriovenous malformations. This does not include cyanoacrylates and other embolic agents, which act by polymerization or precipitation. Embolization devices used in other vascular applications are also not included in this classification, see §870.3300.

(b) Classification. Class II (special controls.) The special control for this device is the FDA guidance document entitled “Class II Special Controls Guidance Document: Vascular and Neurovascular Embolization Devices.” For availability of this guidance document, see §882.1(e).

[69 FR 77900, Dec. 29, 2004]