510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K802869Substantially Equivalent

Backtrac 90-90 Traction

Backtrac, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K802869 is the FDA 510(k) clearance record for BACKTRAC 90-90 TRACTION, a class I device, cleared for Backtrac on under FDA product code KQZ (Component, Traction, Non-Invasive). FDA records list one 510(k) clearance for Backtrac. As of , FDA records show no recalls naming K802869.

Clearance record

Decision date
Received
(27 days to decision)
Product code
KQZ Component, Traction, Non-Invasive
Regulation
21 CFR 888.5890
Device class
Class I
Review panel
Orthopedic
Applicant
Backtrac 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KQZ

Trailing 12 months

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

FDA records show no clearances under product code KQZ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KQZ, 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