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FDA 510(k)

SARGON CYLINDRO-BLADE IMPLANT

K-Number: K930071 · 1994-07-08

ApplicantSargon Ent., Inc.
Decision Date1994-07-08
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SARGON CYLINDRO-BLADE IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Sargon Ent., Inc.. It received FDA 510(k) clearance on 1994-07-08 under 510(k) number K930071. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SARGON CYLINDRO-BLADE IMPLANT?

SARGON CYLINDRO-BLADE IMPLANT is a medical device that received FDA 510(k) clearance on 1994-07-08. The listed applicant is Sargon Ent., Inc.. The 510(k) number is K930071.

When did SARGON CYLINDRO-BLADE IMPLANT receive FDA 510(k) clearance?

SARGON CYLINDRO-BLADE IMPLANT received FDA 510(k) clearance on 1994-07-08, under 510(k) number K930071.

Who is the listed applicant for SARGON CYLINDRO-BLADE IMPLANT?

The FDA 510(k) record lists Sargon Ent., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SARGON CYLINDRO-BLADE IMPLANT?

The FDA product code for SARGON CYLINDRO-BLADE IMPLANT is DZE.

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.

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Other records listing Sargon Ent., Inc. 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.

K082573SARGON NON-EXPANDABLE DENTAL IMPLANTK981141SARGON IMMEDIATE LOAD IMPLANT, MODEL D

Related Devices (Code: DZE)

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.

K261392TriActive Dental Implant SystemParagon Implant Mfg., LLCK260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, Inc.

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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