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FDA 510(k)

STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE

K-Number: K955599 · 1996-02-22

ApplicantStryker Corp.
Decision Date1996-02-22
Product CodeGDY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1996-02-22 under 510(k) number K955599. The device is classified under product code GDY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE?

STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE is a medical device that received FDA 510(k) clearance on 1996-02-22. The listed applicant is Stryker Corp.. The 510(k) number is K955599.

When did STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE receive FDA 510(k) clearance?

STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE received FDA 510(k) clearance on 1996-02-22, under 510(k) number K955599.

Who is the listed applicant for STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE?

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 FEMORAL CANAL SPONGE & ACETABULUM SPONGE?

The FDA product code for STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE is GDY.

Related Clinical Trials

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.

Other records listing Stryker Corp. as applicant

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.

View all 119 devices →

Related Devices (Code: GDY)

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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