510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K911805Substantially Equivalent

Kin-Com Asymmetrical Back System

Chattanooga Group, Inc., Hixson TN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K911805 is the FDA 510(k) clearance record for KIN-COM ASYMMETRICAL BACK SYSTEM, a class II device, cleared for Chattanooga Group, Inc. on under FDA product code IKK (System, Isokinetic Testing And Evaluation). FDA records list 81 510(k) clearances for Chattanooga Group, Inc., from to . As of , FDA records show no recalls naming K911805.

Clearance record

Decision date
Received
(71 days to decision)
Product code
IKK System, Isokinetic Testing And Evaluation
Regulation
21 CFR 890.1925
Device class
Class II
Review panel
Physical Medicine
Applicant
Chattanooga Group, Inc. 4717 Adams Rd., Hixson TN
510(k) summary
Statement
Third party review
No

Clearances, product code IKK

Trailing 12 months

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

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