Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DEVICE PART NUMBER: SVD-3S DRILL

K-Number: K902930 · 1990-11-20

ApplicantMinimatic Implant Technology
Decision Date1990-11-20
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DEVICE PART NUMBER: SVD-3S DRILL is the device name listed in this FDA 510(k) record. The listed applicant is Minimatic Implant Technology. It received FDA 510(k) clearance on 1990-11-20 under 510(k) number K902930. 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 DEVICE PART NUMBER: SVD-3S DRILL?

DEVICE PART NUMBER: SVD-3S DRILL is a medical device that received FDA 510(k) clearance on 1990-11-20. The listed applicant is Minimatic Implant Technology. The 510(k) number is K902930.

When did DEVICE PART NUMBER: SVD-3S DRILL receive FDA 510(k) clearance?

DEVICE PART NUMBER: SVD-3S DRILL received FDA 510(k) clearance on 1990-11-20, under 510(k) number K902930.

Who is the listed applicant for DEVICE PART NUMBER: SVD-3S DRILL?

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

What is the FDA product code for DEVICE PART NUMBER: SVD-3S DRILL?

The FDA product code for DEVICE PART NUMBER: SVD-3S DRILL 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Minimatic Implant Technology 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.

K911776DPI-1106 IMPLANT, MODIFICATIONK903515HH-1119 HEALING HEADK911112DEVICE PART NUMBERS: - 1400 SERIESK905039IMPLANT, THREADED EXTERNAL HEX, TAPERED SHOULDERK904707BC 1208 IMPLANT, THREADED EXTERNAL HEXK903043ICT-1108 IMPLANT- THREADED (CEMENT TYPE ABUTMENT)

View all 34 devices →

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑