Osteoimplant Technology, Inc.
Osteoimplant Technology, Inc. holds FDA 510(k) medical device clearances, first cleared 1996, most recent 2005.
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.