510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K033856Substantially Equivalent

5.0 Cannulated Drill Pin, 6.0 Cannulated Drill-Pin

Peter Stevens, MD, Salt Lake City UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K033856 is the FDA 510(k) clearance record for 5.0 CANNULATED DRILL PIN, 6.0 CANNULATED DRILL-PIN, a class II device, cleared for Peter Stevens, MD on under FDA product code KTT (Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component). FDA records list one 510(k) clearance for Peter Stevens, MD. As of , FDA records show no recalls naming K033856.

Clearance record

Decision date
Received
(393 days to decision)
Product code
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Regulation
21 CFR 888.3030
Device class
Class II
Review panel
Orthopedic
Applicant
Peter Stevens, MD P.O. Box 58246, Salt Lake City UT
510(k) summary
Statement
Third party review
No

Clearances, product code KTT

Trailing 12 months
9 clearances under product code KTT in the twelve months to October 2026, November 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code KTT, trailing twelve months
MonthClearances
November 20252
December 20252
January 20261
February 20260
March 20261
April 20261
May 20260
June 20261
July 20260
August 20260
September 20260
October 20261