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FDA 510(k)

SHORTSTOP DISPOSABLE PROPHY ANGLE

K-Number: K955654 · 1996-02-08

Decision Date1996-02-08
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SHORTSTOP DISPOSABLE PROPHY ANGLE is the device name listed in this FDA 510(k) record. The listed applicant is Spintech, Inc.. It received FDA 510(k) clearance on 1996-02-08 under 510(k) number K955654. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHORTSTOP DISPOSABLE PROPHY ANGLE?

SHORTSTOP DISPOSABLE PROPHY ANGLE is a medical device that received FDA 510(k) clearance on 1996-02-08. The listed applicant is Spintech, Inc.. The 510(k) number is K955654.

When did SHORTSTOP DISPOSABLE PROPHY ANGLE receive FDA 510(k) clearance?

SHORTSTOP DISPOSABLE PROPHY ANGLE received FDA 510(k) clearance on 1996-02-08, under 510(k) number K955654.

Who is the listed applicant for SHORTSTOP DISPOSABLE PROPHY ANGLE?

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

What is the FDA product code for SHORTSTOP DISPOSABLE PROPHY ANGLE?

The FDA product code for SHORTSTOP DISPOSABLE PROPHY ANGLE is EFB.

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 Spintech, 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.

View all 10 devices →

Related Devices (Code: EFB)

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

View on FDA Database →

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

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