510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K952167Substantially Equivalent

Imz Bone Tack System

Interpore Intl., Irvine CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K952167 is the FDA 510(k) clearance record for IMZ BONE TACK SYSTEM, a class II device, cleared for Interpore Intl. on under FDA product code DZL (Screw, Fixation, Intraosseous). FDA records list 25 510(k) clearances for Interpore Intl., from to . As of , FDA records show no recalls naming K952167.

Clearance record

Decision date
Received
(197 days to decision)
Product code
DZL Screw, Fixation, Intraosseous
Regulation
21 CFR 872.4880
Device class
Class II
Review panel
Dental
Applicant
Interpore Intl. 181 Technology Dr., Irvine CA
510(k) summary
Statement
Third party review
No

Clearances, product code DZL

Trailing 12 months
1 clearance under product code DZL in the twelve months to October 2026, August 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DZL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260