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FDA 510(k)

MEMFIX

K-Number: K955369 · 1996-01-23

ApplicantThe Straumann Co.
Decision Date1996-01-23
Product CodeDZL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MEMFIX is the device name listed in this FDA 510(k) record. The listed applicant is The Straumann Co.. It received FDA 510(k) clearance on 1996-01-23 under 510(k) number K955369. The device is classified under product code DZL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEMFIX?

MEMFIX is a medical device that received FDA 510(k) clearance on 1996-01-23. The listed applicant is The Straumann Co.. The 510(k) number is K955369.

When did MEMFIX receive FDA 510(k) clearance?

MEMFIX received FDA 510(k) clearance on 1996-01-23, under 510(k) number K955369.

Who is the listed applicant for MEMFIX?

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

What is the FDA product code for MEMFIX?

The FDA product code for MEMFIX is DZL.

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Other records listing The Straumann Co. as applicant

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K041070STRAUMANN TEMPORARY COPINGK040646STRAUMANN GRANULESK040469THE STRAUMANN ORTHO IMPLANT SYSTEMK993862MODUS SAGITTAL SPLIT PLATEK962023PLASTIC PROTECTION HEALING CAPSK960634TITANIUM HEALING CAPS

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Related Devices (Code: DZL)

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.

K254286Guided Bone Regeneration SystemDentalMaster(Xiamen)Medical Technology Co., Ltd.K250123Master-Pin X (MP Pin with thread) (36BMP000030 / MP30)Hager& Meisinger GmbHK251569Bone ScrewOsstem Implant Co., Ltd.K243190USTOMED Bone Fixation/Bone Augmentation Systems - PINUstomed Instrumente Ulrich Storz GmbH & Co. KGK233419GBR SystemProimtech Saglik Urunleri Anonim SirketiK240321MP Pin flat without thread (36BMP000020/MP20)Hager& Meisinger GmbH

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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