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.

Surgtech, Inc.

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6
Categories6
Latest FDA decision2019-08-01
TypeNumberDevice NameCodeDateActions
510(k) K191192 SurgTech GENOLL Total Knee SystemJWH2019-08-01 View
510(k) K173455 SurgTech Bipolar Head SystemKWY2018-06-14 View
510(k) K162125 MALUC™ Total Hip Arthroplasty SystemJDI2017-05-10 View
510(k) K163363 SurgTech Thoracolumbosacral (TLS) Posterior Fixation SystemNKB2017-04-05 View
510(k) K161894 SurgTech Trauma SystemHWC2017-02-21 View
510(k) K152200 SurgTech Interbody SystemMAX2016-03-25 View