510(k) K870331

IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS by Interpore Intl. — Product Code EGG

K870331 is an FDA 510(k) premarket notification submitted by Interpore Intl. for the device "IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS". The FDA issued a decision of Substantially Equivalent on March 2, 1987. The device falls under product code EGG (Attachment, Precision, All), a Class I device regulated under 21 CFR 872.3165. Interpore Intl. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 2, 1987
Date Received
January 28, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Attachment, Precision, All
Device Class
Class I
Regulation Number
872.3165
Review Panel
DE
Submission Type