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FDA 510(k)

STRYKER SAGITTAL SAW ATTACHMENT

K-Number: K954483 · 1996-01-30

ApplicantStryker Instruments
Decision Date1996-01-30
Product CodeGFA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STRYKER SAGITTAL SAW ATTACHMENT is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Instruments. It received FDA 510(k) clearance on 1996-01-30 under 510(k) number K954483. The device is classified under product code GFA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER SAGITTAL SAW ATTACHMENT?

STRYKER SAGITTAL SAW ATTACHMENT is a medical device that received FDA 510(k) clearance on 1996-01-30. The listed applicant is Stryker Instruments. The 510(k) number is K954483.

When did STRYKER SAGITTAL SAW ATTACHMENT receive FDA 510(k) clearance?

STRYKER SAGITTAL SAW ATTACHMENT received FDA 510(k) clearance on 1996-01-30, under 510(k) number K954483.

Who is the listed applicant for STRYKER SAGITTAL SAW ATTACHMENT?

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

What is the FDA product code for STRYKER SAGITTAL SAW ATTACHMENT?

The FDA product code for STRYKER SAGITTAL SAW ATTACHMENT is GFA.

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Related Devices (Code: GFA)

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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