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FDA 510(k)

STRYKER PATIENT SPECIFIC CUTTING GUIDE

K-Number: K110533 · 2011-05-19

ApplicantStryker Corp.
Decision Date2011-05-19
Product CodeMBH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

STRYKER PATIENT SPECIFIC CUTTING GUIDE is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 2011-05-19 under 510(k) number K110533. The device is classified under product code MBH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER PATIENT SPECIFIC CUTTING GUIDE?

STRYKER PATIENT SPECIFIC CUTTING GUIDE is a medical device that received FDA 510(k) clearance on 2011-05-19. The listed applicant is Stryker Corp.. The 510(k) number is K110533.

When did STRYKER PATIENT SPECIFIC CUTTING GUIDE receive FDA 510(k) clearance?

STRYKER PATIENT SPECIFIC CUTTING GUIDE received FDA 510(k) clearance on 2011-05-19, under 510(k) number K110533.

Who is the listed applicant for STRYKER PATIENT SPECIFIC CUTTING GUIDE?

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

What is the FDA product code for STRYKER PATIENT SPECIFIC CUTTING GUIDE?

The FDA product code for STRYKER PATIENT SPECIFIC CUTTING GUIDE is MBH.

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Other records listing Stryker Corp. as applicant

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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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