Medical Device Manufacturer · US , Walker , MI

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

13 submissions · 11 cleared · Since 1983

Total

Cleared

Denied

Implant Technology, Inc. has 11 FDA 510(k) cleared orthopedic devices. Based in Walker, US.

Historical record: 11 cleared submissions from 1983 to 1995.

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 - Implant Technology, Inc.

13 devices

1-12 of 13

Cleared Jan 11, 1995

HIP JOINT METAL/POLYMER SEMI-CONSTRAINED PROTHESIS

K921525 · LPH

Orthopedic · 1013d

Cleared May 28, 1992

LSF HA COATED FEMORAL HIP

K915617 · MEH

Orthopedic · 164d

Cleared Mar 25, 1992

LSF TOTAL HIP SYSTEM - MULLER-TYPE ACETABULAR CUP

K920021 · JDI

Orthopedic · 83d

Cleared Nov 07, 1991

LSF DIAGNOSTIC RELATED GROUP CEMENTED HIP

K913616 · JDI

Orthopedic · 86d

Cleared Aug 09, 1990

LSF CEMENTED FEMORAL HIP

K902727 · JDI

Orthopedic · 49d

Cleared May 22, 1990

LSF(TM) TOTAL HIP SYSTEM

K901460 · JDI

Orthopedic · 55d

Cleared May 02, 1989

IMPLANT TECHNOLOGY BONE CEMENT EXTRACTOR

K891472 · LZV

Orthopedic · 48d

Cleared Dec 09, 1988

MODIFIED LSF TOTAL HIP SYSTEM

K884432 · JDI

Orthopedic · 49d

Cleared Nov 22, 1988

LSF (R) TOTAL HIP SYSTEM - BIPOLAR COMPONENT

K883212 · KXA

Orthopedic · 116d

Cleared Jun 11, 1986

LSF* TOTAL HIP SYSTEM

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

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