Question 1

Who is the manufacturer of INSULATED HOOK SCISSORS/J & L HOOK KNIVES/SPATULA?

Accepted Answer

Northgate Technologies, Inc. filed the 510(k) submission for INSULATED HOOK SCISSORS/J & L HOOK KNIVES/SPATULA (K911316).

Question 2

What is the FDA product code for INSULATED HOOK SCISSORS/J & L HOOK KNIVES/SPATULA?

Accepted Answer

GEI. It is classified under 21 CFR 878.4400 as a Class 2 device in the General, Plastic Surgery panel.

Question 3

When was INSULATED HOOK SCISSORS/J & L HOOK KNIVES/SPATULA cleared by the FDA?

Accepted Answer

Apr 29, 1991 (decision: SESE).

Question 4

What is the regulatory pathway for INSULATED HOOK SCISSORS/J & L HOOK KNIVES/SPATULA?

Accepted Answer

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

Question 5

Who can help prepare an FDA 510(k) submission like INSULATED HOOK SCISSORS/J & L HOOK KNIVES/SPATULA?

Accepted Answer

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.

Record ID	K911316
Device Name	INSULATED HOOK SCISSORS/J & L HOOK KNIVES/SPATULA
Applicant	Northgate Technologies, Inc.
Product Code	GEI · General, Plastic Surgery
Decision Date	Apr 29, 1991
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 878.4400
Device Class	Class 2

INSULATED HOOK SCISSORS/J & L HOOK KNIVES/SPATULA

Device Facts

Regulatory Classification

Identification