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FDA 510(k)

SELF GUIDING (SG) INTERLOCKING NAIL

K-Number: K880737 · 1988-03-14

ApplicantOrthopaedic Designs, Inc.
Decision Date1988-03-14
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SELF GUIDING (SG) INTERLOCKING NAIL is the device name listed in this FDA 510(k) record. The listed applicant is Orthopaedic Designs, Inc.. It received FDA 510(k) clearance on 1988-03-14 under 510(k) number K880737. 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 SELF GUIDING (SG) INTERLOCKING NAIL?

SELF GUIDING (SG) INTERLOCKING NAIL is a medical device that received FDA 510(k) clearance on 1988-03-14. The listed applicant is Orthopaedic Designs, Inc.. The 510(k) number is K880737.

When did SELF GUIDING (SG) INTERLOCKING NAIL receive FDA 510(k) clearance?

SELF GUIDING (SG) INTERLOCKING NAIL received FDA 510(k) clearance on 1988-03-14, under 510(k) number K880737.

Who is the listed applicant for SELF GUIDING (SG) INTERLOCKING NAIL?

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

What is the FDA product code for SELF GUIDING (SG) INTERLOCKING NAIL?

The FDA product code for SELF GUIDING (SG) INTERLOCKING NAIL is HSB.

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Other records listing Orthopaedic Designs, 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.

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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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