Atlas FDA

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

Medical Metrics, Inc. · Predicate Candidate Screening

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

67 daysmedian FDA review time
134 days90th percentile
5clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K231668Spine CAMP™ (1.1)Medical Metrics, Inc.2023-07-07300
K221632Spine CAMP™Medical Metrics, Inc.2022-10-181340
K022585KIMAX QMAMedical Metrics, Inc.2002-10-11670
K013098KIMAX REMOTE VIEWING STATIONMedical Metrics, Inc.2001-12-07810
K010187KIMAX, MODEL 1024Medical Metrics, Inc.2001-02-14230

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