Interpore Imz(Castable)Tub/Scret Ret Rigid Attach
FDA 510(k) K901928 · Interpore Intl.
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)
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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.