Osteo Technology, Inc.
FDA 510(k) medical device clearances.
Top product codes for Osteo Technology, Inc.
Recent clearances by Osteo Technology, Inc.
- K926156 — REPLICA(TM) TOTAL HIP SYSTEM
- K922859 — ANATOMICAL TYPE KNEE SYSTEM
- K922869 — TOTAL CONDYLAT TYPE KNEE SYSTEM
- K925447 — OTI ORTHOPEDIC WIRE SYSTEM
- K926213 — MODIFIED ZICKEL INTRAMEDULLARY ROD SYSTEM
- K922861 — BIOMETRIC SCREW FIXATION CUP
- K922870 — THREE SPIKE CUP
- K922682 — AMERICANA HIP PROTHESIS
- K925301 — OTI ORTHOPEDIC FASTENER SYSTEM
- K922860 — AUSTIN-MOORE TYPE HIP PROSTHESIS
- K922862 — CHARNLEY TYPE HIP PROTHESIS
- K922863 — EUROSTEM HIP PROTHESIS SYSTEM
- K922864 — MUELLER TYPE FEMORAL STEM
- K922866 — OTI BONE PLUG
- K922868 — THOMPSON TYPE HIP PROTHESIS
- K922871 — UNIFIT FEMORAL STEM
- K922645 — LSF ANATOMIC CEMENTED HIP
- K922865 — NEER TYPE SHOULDER PROSTHESIS SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.