Osteo Technology, Inc.
Osteo Technology, Inc. holds FDA 510(k) medical device clearances, first cleared 1992, most recent 1994.
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.