Medical Device Manufacturer · US , Mchenry , IL

Intermedics Orthopedics - FDA 510(k) Cleared Devices

108 submissions · 82 cleared · Since 1982

108

Total

Cleared

Denied

Intermedics Orthopedics has 82 FDA 510(k) cleared orthopedic devices. Based in Mchenry, US.

Historical record: 82 cleared submissions from 1982 to 1997.

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 - Intermedics Orthopedics

108 devices

1-12 of 108

Cleared Jul 03, 1997

NATURAL-HIP SYSTEM POROUS STEM WITH HA/CSTI

K970300 · LPH

Orthopedic · 160d

Cleared Apr 30, 1997

NATURAL-KNEE II REVISION FEMORAL SPACER LUGS

K970498 · JWH

Orthopedic · 79d

Cleared Apr 08, 1997

NATURAL-HIP SYSTEM COCR REVISION STEM

K970166 · LZO

Orthopedic · 82d

Cleared Feb 27, 1997

SELECT SHOULDER CURVED-BACK PEGGED ALL POLY GLENOIDS

K970567 · KWT

Orthopedic · 14d

Cleared Jan 27, 1997

NATURAL-HIP SYSTEM COCR STEM

K964357 · LZO

Orthopedic · 87d

Cleared Jan 16, 1997

MODULA OPTIONS FOR SEVERE BONE LOSS AND TRAUMA

K964350 · JDI

Orthopedic · 77d

Cleared Oct 28, 1996

PATELLOFEMORAL JOINT PROSTHESIS

K962190 · KRR

Orthopedic · 144d

Cleared Oct 15, 1996

NATURAL HIP SYSTEM POROUS STEM - COLLARLESS, COLLARED

K963266 · LPH

Orthopedic · 56d

Cleared Oct 01, 1996

INTERMOORE FRACTURE HIP STEM (MODIFY)

K963155 · LWJ

Orthopedic · 57d

Cleared Sep 03, 1996

SELECT SHOULDER COCR HUMERAL STEM COMPONENT

K962315 · KWT

Orthopedic · 78d

Cleared Aug 29, 1996

SELECT SHOULDER COCR HUMERAL STEM COMPONENT

K962289 · HSD

Orthopedic · 76d

Cleared Aug 28, 1996

SELECT SHOULDER CONCENTRIC HUMERAL HEAD COMPONENTS

K962224 · KWS

Orthopedic · 79d

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Intermedics Orthopedics - FDA 510(k) Cleared Devices

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