Interpore Imz(Castable)Tub/Scret Ret Rigid Attach

FDA 510(k) K901928 · Interpore Intl.

Substantially Equivalent

510(k) numberK901928

Submission

Device name
Interpore Imz(Castable)Tub/Scret Ret Rigid Attach
Applicant
Interpore Intl.
Rockville, MD, US
Received
April 27, 1990
Decision date
July 26, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
EGG – Attachment, Precision, All
Device class
Class I (low risk)
Regulation
21 CFR 872.3165
Specialty
Dental

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Questions and answers

When was Interpore Imz(Castable)Tub/Scret Ret Rigid Attach cleared by the FDA?

Interpore Imz(Castable)Tub/Scret Ret Rigid Attach (K901928) received a 510(k) decision of Substantially Equivalent on July 26, 1990, 90 days after the submission was received.

What is the product code of K901928?

The FDA product code is EGG – Attachment, Precision, All, a Class I (low risk) device regulated under 21 CFR 872.3165.