STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE
K-Number: K955599 · 1996-02-22
Advertisement
Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement