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

The Progressive Orthopaedic Company, LLC · Predicate Candidate Screening

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

105 daysmedian FDA review time
426 days90th percentile
5clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K183344The Progressive Orthopaedic Company Total Knee System IIThe Progressive Orthopaedic Company, LLC2019-03-181050
K151424The Progressive Orthopaedic Total Hip SystemThe Progressive Orthopaedic Company, LLC2016-07-274260
K150783Progressive Orthopaedic Total Knee SystemThe Progressive Orthopaedic Company, LLC2015-06-23900
K142649Progressive Orthopedic Total Knee SystemThe Progressive Orthopaedic Company, LLC2015-03-241880
K143314Progressive Orthopaedic Total Hip SystemThe Progressive Orthopaedic Company, LLC2015-02-271000

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