Who is the manufacturer of MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATION?

Britt Corp., Inc. filed the 510(k) submission for MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATION (K860977).

What is the FDA product code for MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATION?

LLF. as a Class 3 device in the NE panel.

What is the regulatory pathway for MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATION?

510(k) clearance (submission type: Traditional).

Who can help prepare an FDA 510(k) submission like MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATION?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATION

K860977 · Britt Corp., Inc. · LLF · Oct 16, 1986 · NE

Device Facts

Record ID	K860977
Device Name	MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATION
Applicant	Britt Corp., Inc.
Product Code	LLF · NE
Decision Date	Oct 16, 1986
Decision	SESE
Submission Type	Traditional
Device Class	Class 3

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