Medical Device Manufacturer · US , Pine Brook , NJ

Implantology Corp. - FDA 510(k) Cleared Devices

9 submissions · 7 cleared · Since 1993

Total

Cleared

Denied

Implantology Corp. has 7 FDA 510(k) cleared medical devices. Based in Pine Brook, US.

Historical record: 7 cleared submissions from 1993 to 1994. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Implantology Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Implantology Corp.

9 devices

1-9 of 9

Cleared Jul 22, 1994

UFC HIP STEM COMPONENTS: HYDROXYLAPATITE COATED

K934729 · MEH

Orthopedic · 296d

Cleared Jul 13, 1993

FPC/SFPC/RFPC ACETABULAR COMPONENT

K915529 · JDL

Orthopedic · 581d

Cleared Jun 29, 1993

BHR BIPOLAR FEMORAL HEAD COMPONENT

K915528 · LZY

Orthopedic · 567d

Cleared Jun 24, 1993

CPS ACETABULAR COMPONENT

K915527 · JDL

Orthopedic · 562d

Cleared May 17, 1993

PPC HIP STEM COMPONENT

K915385 · JDG

Orthopedic · 535d

Cleared Apr 30, 1993

FPC HIP STEM COMPONENT

K915391 · JDG

Orthopedic · 518d

Cleared Apr 30, 1993

UFC HIP STEM COMPONENT

K924099 · JDG

Orthopedic · 260d

Cleared Mar 04, 1993

PSK POSTERIOR STABILIZED TOATAL KNEE

K915798 · JWH

Orthopedic · 436d

Cleared Feb 12, 1993

CRK CONDYLAR RESURFACING TOTAL KNEE

K915584 · JWH

Orthopedic · 427d

Implantology Corp. - FDA 510(k) Cleared Devices

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