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FDA 510(k)

IMCOR 3.75 MM WIDE HEX SELF-TAPPING SCREW W/COVER SCREW

K-Number: K960900 · 1996-06-05

ApplicantImcor
Decision Date1996-06-05
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMCOR 3.75 MM WIDE HEX SELF-TAPPING SCREW W/COVER SCREW is the device name listed in this FDA 510(k) record. The listed applicant is Imcor. It received FDA 510(k) clearance on 1996-06-05 under 510(k) number K960900. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMCOR 3.75 MM WIDE HEX SELF-TAPPING SCREW W/COVER SCREW?

IMCOR 3.75 MM WIDE HEX SELF-TAPPING SCREW W/COVER SCREW is a medical device that received FDA 510(k) clearance on 1996-06-05. The listed applicant is Imcor. The 510(k) number is K960900.

When did IMCOR 3.75 MM WIDE HEX SELF-TAPPING SCREW W/COVER SCREW receive FDA 510(k) clearance?

IMCOR 3.75 MM WIDE HEX SELF-TAPPING SCREW W/COVER SCREW received FDA 510(k) clearance on 1996-06-05, under 510(k) number K960900.

Who is the listed applicant for IMCOR 3.75 MM WIDE HEX SELF-TAPPING SCREW W/COVER SCREW?

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

What is the FDA product code for IMCOR 3.75 MM WIDE HEX SELF-TAPPING SCREW W/COVER SCREW?

The FDA product code for IMCOR 3.75 MM WIDE HEX SELF-TAPPING SCREW W/COVER SCREW is DZE.

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 Imcor 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.

View all 7 devices →

Related Devices (Code: DZE)

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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