Osteoimplant Technology, Inc.
FDA 510(k) medical device clearances.
Top product codes for Osteoimplant Technology, Inc.
Recent clearances by Osteoimplant Technology, Inc.
- K040685 — Z - SERIES MODULAR TOTAL HIP SYSTEM PLASMA COATED
- K041443 — OTI ALUMINA CERAMIC FEMORAL HEAD SYSTEM
- K040225 — OTI ALUMINA CERAMIC FEMORAL HEAD SYSTEM
- K032729 — Z-SERIES MODULAR TOTAL HIP SYSTEM
- K030608 — OTI BONE CEMENT PLUG
- K022779 — OTI UNICONDULAR INTERPOSITIONAL SPACER
- K021822 — R120 MODULAR TOTAL HIP SYSTEM
- K012762 — MJS POSTERIOR STABILIZED KNEE SYSTEM
- K011774 — R120 MODULAR TOTAL HIP SYSTEM
- K003316 — OTI CERAMIC FEMORAL HEAD SYSTEM
- K003199 — TRIAD II MODULAR TOTAL HIP SYSTEM
- K000817 — OMEGA II MODULAR TOTAL HIP SYSTEM
- K984227 — OMEGA II MODULAR TOTAL HIP SYSTEM
- K990003 — J-SERIES OMEGA TOTAL HIP SYSTEM
- K982886 — OTI MODULAR SHOULDER SYSTEM
- K982598 — OTI FEMORAL LOCK TOTAL HIP SYSTEM
- K980981 — OMEGA HA COATED TOTAL HIP SYSTEM
- K974506 — LSF HA COATED TRIAD TOTAL HIP SYSTEM
- K971020 — LSF TRIAD TOTAL HIP SYSTEM
- K964924 — OMEGA TOTAL HIP SYSTEM FOR USE WITHOUT BONE CEMENT (LINE EXTENSION)
- K960647 — OMEGA TOTAL HIP SYSTEM FOR CEMENTED APPLICATIONS
Data sourced from openFDA. This site is unofficial and independent of the FDA.