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FDA 510(k)

5.0 CANNULATED DRILL PIN, 6.0 CANNULATED DRILL-PIN

K-Number: K033856 · 2005-01-07

ApplicantPeter Stevens, MD
Decision Date2005-01-07
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

5.0 CANNULATED DRILL PIN, 6.0 CANNULATED DRILL-PIN is the device name listed in this FDA 510(k) record. The listed applicant is Peter Stevens, MD. It received FDA 510(k) clearance on 2005-01-07 under 510(k) number K033856. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 5.0 CANNULATED DRILL PIN, 6.0 CANNULATED DRILL-PIN?

5.0 CANNULATED DRILL PIN, 6.0 CANNULATED DRILL-PIN is a medical device that received FDA 510(k) clearance on 2005-01-07. The listed applicant is Peter Stevens, MD. The 510(k) number is K033856.

When did 5.0 CANNULATED DRILL PIN, 6.0 CANNULATED DRILL-PIN receive FDA 510(k) clearance?

5.0 CANNULATED DRILL PIN, 6.0 CANNULATED DRILL-PIN received FDA 510(k) clearance on 2005-01-07, under 510(k) number K033856.

Who is the listed applicant for 5.0 CANNULATED DRILL PIN, 6.0 CANNULATED DRILL-PIN?

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

What is the FDA product code for 5.0 CANNULATED DRILL PIN, 6.0 CANNULATED DRILL-PIN?

The FDA product code for 5.0 CANNULATED DRILL PIN, 6.0 CANNULATED DRILL-PIN is KTT.

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Related Devices (Code: KTT)

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

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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