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FDA 510(k)

BAUMER PINS

K-Number: K930969 · 1994-03-29

Decision Date1994-03-29
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BAUMER PINS is the device name listed in this FDA 510(k) record. The listed applicant is Baumer Ortopedia , Ltd.. It received FDA 510(k) clearance on 1994-03-29 under 510(k) number K930969. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BAUMER PINS?

BAUMER PINS is a medical device that received FDA 510(k) clearance on 1994-03-29. The listed applicant is Baumer Ortopedia , Ltd.. The 510(k) number is K930969.

When did BAUMER PINS receive FDA 510(k) clearance?

BAUMER PINS received FDA 510(k) clearance on 1994-03-29, under 510(k) number K930969.

Who is the listed applicant for BAUMER PINS?

The FDA 510(k) record lists Baumer Ortopedia , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BAUMER PINS?

The FDA product code for BAUMER PINS is HTY.

Related Clinical Trials

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.

Other records listing Baumer Ortopedia , Ltd. as applicant

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.

Related Devices (Code: HTY)

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.

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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