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Found 2 results

510(k) Data Aggregation

K Number

Device Name

K-WIRE

Manufacturer

AMERICAN MEDICAL SPECIALTIES, INC.

Date Cleared

1996-04-09

(67 days)

Product Code

Regulation Number

Why did this record match?

Applicant Name (Manufacturer) :

AMERICAN MEDICAL SPECIALTIES, INC.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

Intended Use

Device Description

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K Number

Device Name

STEINMAN PIN

Manufacturer

AMERICAN MEDICAL SPECIALTIES, INC.

Date Cleared

1996-04-09

(67 days)

Product Code

Regulation Number

Why did this record match?

Applicant Name (Manufacturer) :

AMERICAN MEDICAL SPECIALTIES, INC.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

Intended Use

Device Description

Ask a Question

Ask a specific question about this device

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