510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K213982Substantially Equivalent

Pacific Instruments Orthopedic Fixation Pins and Wires / Kirschner / Guide Wires

Pacific Instruments Inc., Honolulu HI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K213982 is the FDA 510(k) clearance record for Pacific Instruments Orthopedic Fixation Pins and Wires / Kirschner / Guide Wires, a class II device, cleared for Pacific Instruments on under FDA product code HTY (Pin, Fixation, Smooth). FDA records list one 510(k) clearance for Pacific Instruments. As of , FDA records show no recalls naming K213982.

Clearance record

Decision date
Received
(59 days to decision)
Product code
HTY Pin, Fixation, Smooth
Regulation
21 CFR 888.3040
Device class
Class II
Review panel
Orthopedic
Applicant
Pacific Instruments 438 Hobron Ln., Suite 204, Honolulu HI
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HTY

Trailing 12 months
2 clearances under product code HTY in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HTY, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260