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FDA 510(k)

STRYKER CROSS-PINNED INTERFERENCE SCREW SYSTEM

K-Number: K012270 · 2001-09-28

ApplicantStryker Endoscopy
Decision Date2001-09-28
Product CodeJDW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

STRYKER CROSS-PINNED INTERFERENCE SCREW 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 2001-09-28 under 510(k) number K012270. 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 CROSS-PINNED INTERFERENCE SCREW SYSTEM?

STRYKER CROSS-PINNED INTERFERENCE SCREW SYSTEM is a medical device that received FDA 510(k) clearance on 2001-09-28. The listed applicant is Stryker Endoscopy. The 510(k) number is K012270.

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

STRYKER CROSS-PINNED INTERFERENCE SCREW SYSTEM received FDA 510(k) clearance on 2001-09-28, under 510(k) number K012270.

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

The FDA product code for STRYKER CROSS-PINNED INTERFERENCE SCREW 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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