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FDA 510(k)

OGDEN ANCHOR

K-Number: K924367 · 1993-07-26

ApplicantAdvanced Surgical Implants, Inc.
Decision Date1993-07-26
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OGDEN ANCHOR is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Surgical Implants, Inc.. It received FDA 510(k) clearance on 1993-07-26 under 510(k) number K924367. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OGDEN ANCHOR?

OGDEN ANCHOR is a medical device that received FDA 510(k) clearance on 1993-07-26. The listed applicant is Advanced Surgical Implants, Inc.. The 510(k) number is K924367.

When did OGDEN ANCHOR receive FDA 510(k) clearance?

OGDEN ANCHOR received FDA 510(k) clearance on 1993-07-26, under 510(k) number K924367.

Who is the listed applicant for OGDEN ANCHOR?

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

What is the FDA product code for OGDEN ANCHOR?

The FDA product code for OGDEN ANCHOR is JDR.

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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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