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FDA 510(k)

GLOBAL PRESS-FIT STEM

K-Number: K032385 · 2003-10-30

ApplicantGlobal Medical Co.
Decision Date2003-10-30
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

GLOBAL PRESS-FIT STEM is the device name listed in this FDA 510(k) record. The listed applicant is Global Medical Co.. It received FDA 510(k) clearance on 2003-10-30 under 510(k) number K032385. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLOBAL PRESS-FIT STEM?

GLOBAL PRESS-FIT STEM is a medical device that received FDA 510(k) clearance on 2003-10-30. The listed applicant is Global Medical Co.. The 510(k) number is K032385.

When did GLOBAL PRESS-FIT STEM receive FDA 510(k) clearance?

GLOBAL PRESS-FIT STEM received FDA 510(k) clearance on 2003-10-30, under 510(k) number K032385.

Who is the listed applicant for GLOBAL PRESS-FIT STEM?

The FDA 510(k) record lists Global Medical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GLOBAL PRESS-FIT STEM?

The FDA product code for GLOBAL PRESS-FIT STEM is LPH.

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Related Devices (Code: LPH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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