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FDA 510(k)

IMZ BONE TACK SYSTEM

K-Number: K952167 · 1995-11-21

ApplicantInterpore Intl.
Decision Date1995-11-21
Product CodeDZL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMZ BONE TACK SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Interpore Intl.. It received FDA 510(k) clearance on 1995-11-21 under 510(k) number K952167. 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 IMZ BONE TACK SYSTEM?

IMZ BONE TACK SYSTEM is a medical device that received FDA 510(k) clearance on 1995-11-21. The listed applicant is Interpore Intl.. The 510(k) number is K952167.

When did IMZ BONE TACK SYSTEM receive FDA 510(k) clearance?

IMZ BONE TACK SYSTEM received FDA 510(k) clearance on 1995-11-21, under 510(k) number K952167.

Who is the listed applicant for IMZ BONE TACK SYSTEM?

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

What is the FDA product code for IMZ BONE TACK SYSTEM?

The FDA product code for IMZ BONE TACK SYSTEM is DZL.

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Other records listing Interpore Intl. 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.

K981253ULTRACON ULTRAFILTRATORK980817PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE MODEL NUMBERS 5RG05, 5RG10, 5RG15, 5G15L, 5RG20, 5RG30, 5RG30LK972842INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGEK971036ODONTIT AUTOGENOUS BONE COLLECTION DEVICEK960945IMZ MEMBRANE TACK SYSTEMK960371INTERPORE THREADED IMPLANT

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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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