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Found 2 results

510(k) Data Aggregation

K Number

Validate with FDA (Live)

Device Name

ARTHOPOR I & II ACETABULAR CUP/ARTHOPOR II OBLONG ACETABULAR CUP

Manufacturer

JOINT MEDICAL PRODUCTS CORP.

Date Cleared

1996-02-26

(84 days)

Product Code

Regulation Number

Type

Panel

Age Range

N/A

Reference & Predicate Devices

N/A

Predicate For

K983014,K991807

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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K Number

Validate with FDA (Live)

Device Name

S-ROM FEMORAL HIP STEM - SIZE 14 X 8

Manufacturer

JOINT MEDICAL PRODUCTS CORP.

Date Cleared

1996-01-22

(87 days)

Product Code

Regulation Number

Type

Panel

Age Range

N/A

Reference & Predicate Devices

N/A

Predicate For

K000788,K032730,K042127,K052426,K162303,K961939,K974331

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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Ask a specific question about this device

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