Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Gatewood and Associates, Ltd.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K884515 BONE FILE, SELDIN, #11-TSK BONE FILE, DOUBLE-ENDEDEKJ1989-01-10 View
510(k) K884514 FORCEPS, TOWEL, BACKHAUS-TSK (BRAND) TOWELGEN1988-11-17 View
↑