HySil Impression Materials

FDA 510(k) K170736 · Osstem Implant Co., Ltd.

Substantially Equivalent

510(k) numberK170736

Submission

Device name
HySil Impression Materials
Applicant
Osstem Implant Co., Ltd.
Busan, KR
Received
March 10, 2017
Decision date
June 7, 2017
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
ELW – Material, Impression
Device class
Class II (moderate risk)
Regulation
21 CFR 872.3660
Specialty
Dental

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Questions and answers

When was HySil Impression Materials cleared by the FDA?

HySil Impression Materials (K170736) received a 510(k) decision of Substantially Equivalent on June 7, 2017, 89 days after the submission was received.

What is the product code of K170736?

The FDA product code is ELW – Material, Impression, a Class II (moderate risk) device regulated under 21 CFR 872.3660.