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FDA 510(k)

SIMPLER TOADSTOOL ABUTMENT, MODEL S19000-S19009

K-Number: K093975 · 2010-06-04

ApplicantPan Global Implant
Decision Date2010-06-04
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SIMPLER TOADSTOOL ABUTMENT, MODEL S19000-S19009 is the device name listed in this FDA 510(k) record. The listed applicant is Pan Global Implant. It received FDA 510(k) clearance on 2010-06-04 under 510(k) number K093975. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIMPLER TOADSTOOL ABUTMENT, MODEL S19000-S19009?

SIMPLER TOADSTOOL ABUTMENT, MODEL S19000-S19009 is a medical device that received FDA 510(k) clearance on 2010-06-04. The listed applicant is Pan Global Implant. The 510(k) number is K093975.

When did SIMPLER TOADSTOOL ABUTMENT, MODEL S19000-S19009 receive FDA 510(k) clearance?

SIMPLER TOADSTOOL ABUTMENT, MODEL S19000-S19009 received FDA 510(k) clearance on 2010-06-04, under 510(k) number K093975.

Who is the listed applicant for SIMPLER TOADSTOOL ABUTMENT, MODEL S19000-S19009?

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

What is the FDA product code for SIMPLER TOADSTOOL ABUTMENT, MODEL S19000-S19009?

The FDA product code for SIMPLER TOADSTOOL ABUTMENT, MODEL S19000-S19009 is NHA.

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.

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Other records listing Pan Global Implant 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.

K092674SIMPLER TOADSTOOL MINI IMPLANT

Related Devices (Code: NHA)

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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