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FDA 510(k)

HARPOON SUTURE ANCHOR

K-Number: K926037 · 1993-05-05

ApplicantBiomet, Inc.
Decision Date1993-05-05
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HARPOON SUTURE ANCHOR is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 1993-05-05 under 510(k) number K926037. 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 HARPOON SUTURE ANCHOR?

HARPOON SUTURE ANCHOR is a medical device that received FDA 510(k) clearance on 1993-05-05. The listed applicant is Biomet, Inc.. The 510(k) number is K926037.

When did HARPOON SUTURE ANCHOR receive FDA 510(k) clearance?

HARPOON SUTURE ANCHOR received FDA 510(k) clearance on 1993-05-05, under 510(k) number K926037.

Who is the listed applicant for HARPOON SUTURE ANCHOR?

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

What is the FDA product code for HARPOON SUTURE ANCHOR?

The FDA product code for HARPOON SUTURE ANCHOR is JDR.

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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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