Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Chattanooga Group — Predicate Candidate Screening

11 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

109 daysmedian FDA review time
239 days90th percentile
11clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K090632COMPEX REHABChattanooga Group2009-06-01840
K083433INTELECT SWD 100, MODEL 1600; SENIOR SOLUTIONS SHORTWAVE DIAChattanooga Group2009-03-181181
K083140COMPEX SPORT PLUSChattanooga Group2009-02-091090
K070425VITALSTIM EXPERIAChattanooga Group2007-06-111180
K053223TRITON/TRU-TRAC/TX/TRITON DTS TRACTIONChattanooga Group2006-02-24990
K051938TRITON/TRU-TRAC/TX TRACTION DEVICESChattanooga Group2005-09-21650
K040662VECTRA GENISYS (MODULE & TRANSPORTABLE) AND INTELECT XT (MODChattanooga Group2004-09-081800
K040285VECTRA TRANSPORTABLE COMBO AND STIM (SPECIALTY LINE DEALERS)Chattanooga Group2004-04-12661
K031077VECTRA EPR SYSTEM AND INTELECT EPR SYSTEMChattanooga Group2003-12-1125117
K031116VECTRA (INTELECT) EPR ULTRASOUNDChattanooga Group2003-12-032391
K023347VITAL STIMChattanooga Group2002-12-06600

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda