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FDA 510(k)

STEINMAN PIN

K-Number: K960483 · 1996-04-09

ApplicantAmerican Medical Specialties, Inc.
Decision Date1996-04-09
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

STEINMAN PIN is the device name listed in this FDA 510(k) record. The listed applicant is American Medical Specialties, Inc.. It received FDA 510(k) clearance on 1996-04-09 under 510(k) number K960483. 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 STEINMAN PIN?

STEINMAN PIN is a medical device that received FDA 510(k) clearance on 1996-04-09. The listed applicant is American Medical Specialties, Inc.. The 510(k) number is K960483.

When did STEINMAN PIN receive FDA 510(k) clearance?

STEINMAN PIN received FDA 510(k) clearance on 1996-04-09, under 510(k) number K960483.

Who is the listed applicant for STEINMAN PIN?

The FDA 510(k) record lists American Medical Specialties, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STEINMAN PIN?

The FDA product code for STEINMAN PIN 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.

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Other records listing American Medical Specialties, Inc. 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.

K960482K-WIREK934603SURGICAL SAW BLADESK934583BURRS

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.

K262722Primal K-Wire (P99-193-1410)Paragon 28, Inc.K253325ZipToe™ Hammertoe Fusion SystemToetal SolutionsK252657Impact PEEK Union Nail SystemNvision Biomedical Technologies, Inc.K250315RONAVIS – FX (FX-001)AIRS, Inc.K251362PediFlex™ Flexible Nail SystemOrthoPediatrics Corp.K250646Impact PEEK Union Nail SystemNvision Biomedical Technologies

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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