510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K882407Substantially Equivalent

Bow & Arrow Drill Guide

Instrument Makar, Inc., Okemos MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K882407 is the FDA 510(k) clearance record for BOW & ARROW DRILL GUIDE, a class I device, cleared for Instrument Makar, Inc. on under FDA product code LXI (Guide, Drill, Ligament). FDA records list 28 510(k) clearances for Instrument Makar, Inc., from to . As of , FDA records show no recalls naming K882407.

Clearance record

Decision date
Received
(88 days to decision)
Product code
LXI Guide, Drill, Ligament
Regulation
21 CFR 878.4820
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Instrument Makar, Inc. 2950 E. Mt. Hope Rd., Okemos MI
Third party review
No

Clearances, product code LXI

Trailing 12 months

FDA records hold no clearances under product code LXI in the trailing twelve months.

FDA records show no clearances under product code LXI in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LXI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260