510(k) K870331
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