Medical Device Manufacturer · US , Timonium , MD

Osteo Technology, Inc. - FDA 510(k) Cleared Devices

18 submissions · 17 cleared · Since 1992

Total

Cleared

Denied

Osteo Technology, Inc. has 17 FDA 510(k) cleared orthopedic devices. Based in Timonium, US.

Historical record: 17 cleared submissions from 1992 to 1994.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Osteo Technology, Inc.

18 devices

1-18 of 18

Cleared Mar 09, 1994

REPLICA(TM) TOTAL HIP SYSTEM

K926156 · LPH

Orthopedic · 457d

Cleared Sep 23, 1993

ANATOMICAL TYPE KNEE SYSTEM

K922859 · JWH

Orthopedic · 476d

Cleared Jul 13, 1993

TOTAL CONDYLAT TYPE KNEE SYSTEM

K922869 · JWH

Orthopedic · 404d

Cleared Jun 29, 1993

OTI ORTHOPEDIC WIRE SYSTEM

K925447 · JDQ

Orthopedic · 244d

Cleared Jun 17, 1993

MODIFIED ZICKEL INTRAMEDULLARY ROD SYSTEM

K926213 · HSB

Orthopedic · 189d

Cleared May 12, 1993

BIOMETRIC SCREW FIXATION CUP

AMERICANA HIP PROTHESIS

K922682 · JDG

Orthopedic · 285d

Cleared Mar 16, 1993

OTI ORTHOPEDIC FASTENER SYSTEM

K925301 · HTY

Orthopedic · 146d

Cleared Feb 12, 1993

AUSTIN-MOORE TYPE HIP PROSTHESIS

K922860 · JDI

Orthopedic · 253d

Cleared Feb 12, 1993

CHARNLEY TYPE HIP PROTHESIS

K922862 · JDI

Orthopedic · 253d

Cleared Feb 12, 1993

EUROSTEM HIP PROTHESIS SYSTEM

K922863 · JDI

Orthopedic · 253d

Cleared Feb 12, 1993

MUELLER TYPE FEMORAL STEM

THOMPSON TYPE HIP PROTHESIS

LSF ANATOMIC CEMENTED HIP

K922645 · JDI

Orthopedic · 218d

Cleared Dec 10, 1992

NEER TYPE SHOULDER PROSTHESIS SYSTEM

K922865 · KWT

Orthopedic · 189d

Osteo Technology, Inc. - FDA 510(k) Cleared Devices

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