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FDA 510(k)

MODIFICATION TO: STRYKER SPINE OASYS SYSTEM

K-Number: K052317 · 2005-09-21

ApplicantStryker Spine
Decision Date2005-09-21
Product CodeMNI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO: STRYKER SPINE OASYS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Spine. It received FDA 510(k) clearance on 2005-09-21 under 510(k) number K052317. The device is classified under product code MNI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO: STRYKER SPINE OASYS SYSTEM?

MODIFICATION TO: STRYKER SPINE OASYS SYSTEM is a medical device that received FDA 510(k) clearance on 2005-09-21. The listed applicant is Stryker Spine. The 510(k) number is K052317.

When did MODIFICATION TO: STRYKER SPINE OASYS SYSTEM receive FDA 510(k) clearance?

MODIFICATION TO: STRYKER SPINE OASYS SYSTEM received FDA 510(k) clearance on 2005-09-21, under 510(k) number K052317.

Who is the listed applicant for MODIFICATION TO: STRYKER SPINE OASYS SYSTEM?

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

What is the FDA product code for MODIFICATION TO: STRYKER SPINE OASYS SYSTEM?

The FDA product code for MODIFICATION TO: STRYKER SPINE OASYS SYSTEM is MNI.

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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.

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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