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FDA 510(k)

STRYKER INTERFERENCE SCREW CROSS PIN SYSTEM

K-Number: K020097 · 2002-03-15

ApplicantStryker Endoscopy
Decision Date2002-03-15
Product CodeJDW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

STRYKER INTERFERENCE SCREW CROSS PIN SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Endoscopy. It received FDA 510(k) clearance on 2002-03-15 under 510(k) number K020097. The device is classified under product code JDW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER INTERFERENCE SCREW CROSS PIN SYSTEM?

STRYKER INTERFERENCE SCREW CROSS PIN SYSTEM is a medical device that received FDA 510(k) clearance on 2002-03-15. The listed applicant is Stryker Endoscopy. The 510(k) number is K020097.

When did STRYKER INTERFERENCE SCREW CROSS PIN SYSTEM receive FDA 510(k) clearance?

STRYKER INTERFERENCE SCREW CROSS PIN SYSTEM received FDA 510(k) clearance on 2002-03-15, under 510(k) number K020097.

Who is the listed applicant for STRYKER INTERFERENCE SCREW CROSS PIN SYSTEM?

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

What is the FDA product code for STRYKER INTERFERENCE SCREW CROSS PIN SYSTEM?

The FDA product code for STRYKER INTERFERENCE SCREW CROSS PIN SYSTEM is JDW.

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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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