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FDA 510(k)

MAGNUM NAIL

K-Number: K093089 · 2009-11-13

ApplicantRobert Reid, Inc.
Decision Date2009-11-13
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MAGNUM NAIL is the device name listed in this FDA 510(k) record. The listed applicant is Robert Reid, Inc.. It received FDA 510(k) clearance on 2009-11-13 under 510(k) number K093089. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGNUM NAIL?

MAGNUM NAIL is a medical device that received FDA 510(k) clearance on 2009-11-13. The listed applicant is Robert Reid, Inc.. The 510(k) number is K093089.

When did MAGNUM NAIL receive FDA 510(k) clearance?

MAGNUM NAIL received FDA 510(k) clearance on 2009-11-13, under 510(k) number K093089.

Who is the listed applicant for MAGNUM NAIL?

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

What is the FDA product code for MAGNUM NAIL?

The FDA product code for MAGNUM NAIL is HSB.

Related Clinical Trials

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Other records listing Robert Reid, 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.

K093833KAPSS SPINAL SYSTEM

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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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