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FDA 510(k)

MEMODYN STAPLE

K-Number: K002695 · 2001-06-13

ApplicantTelos Medical Equipment
Decision Date2001-06-13
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MEMODYN STAPLE is the device name listed in this FDA 510(k) record. The listed applicant is Telos Medical Equipment. It received FDA 510(k) clearance on 2001-06-13 under 510(k) number K002695. 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 MEMODYN STAPLE?

MEMODYN STAPLE is a medical device that received FDA 510(k) clearance on 2001-06-13. The listed applicant is Telos Medical Equipment. The 510(k) number is K002695.

When did MEMODYN STAPLE receive FDA 510(k) clearance?

MEMODYN STAPLE received FDA 510(k) clearance on 2001-06-13, under 510(k) number K002695.

Who is the listed applicant for MEMODYN STAPLE?

The FDA 510(k) record lists Telos Medical Equipment as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEMODYN STAPLE?

The FDA product code for MEMODYN STAPLE is JDR.

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Related Devices (Code: JDR)

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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