Spartan SC 069

FDA 510(k) K220716 · Spartan Micro, Inc.

Substantially Equivalent

510(k) numberK220716

Submission

Device name
Spartan SC 069
Applicant
Spartan Micro, Inc.
Costa Mesa, CA, US
Received
March 11, 2022
Decision date
May 5, 2022
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DQY – Catheter, Percutaneous
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1250
Specialty
Cardiovascular

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Questions and answers

When was Spartan SC 069 cleared by the FDA?

Spartan SC 069 (K220716) received a 510(k) decision of Substantially Equivalent on May 5, 2022, 55 days after the submission was received.

What is the product code of K220716?

The FDA product code is DQY – Catheter, Percutaneous, a Class II (moderate risk) device regulated under 21 CFR 870.1250.