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FDA 510(k)

DRG MF TITANIUN ALLOY BONE SCREW 1.0MM, 1.2MM, 1.3MM, 1.5MM, 1.7MM, 2.0MM, 2.4MM

K-Number: K974817 · 1998-03-13

ApplicantDoctor'S Research Group, Inc.
Decision Date1998-03-13
Product CodeDZL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DRG MF TITANIUN ALLOY BONE SCREW 1.0MM, 1.2MM, 1.3MM, 1.5MM, 1.7MM, 2.0MM, 2.4MM is the device name listed in this FDA 510(k) record. The listed applicant is Doctor'S Research Group, Inc.. It received FDA 510(k) clearance on 1998-03-13 under 510(k) number K974817. 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 DRG MF TITANIUN ALLOY BONE SCREW 1.0MM, 1.2MM, 1.3MM, 1.5MM, 1.7MM, 2.0MM, 2.4MM?

DRG MF TITANIUN ALLOY BONE SCREW 1.0MM, 1.2MM, 1.3MM, 1.5MM, 1.7MM, 2.0MM, 2.4MM is a medical device that received FDA 510(k) clearance on 1998-03-13. The listed applicant is Doctor'S Research Group, Inc.. The 510(k) number is K974817.

When did DRG MF TITANIUN ALLOY BONE SCREW 1.0MM, 1.2MM, 1.3MM, 1.5MM, 1.7MM, 2.0MM, 2.4MM receive FDA 510(k) clearance?

DRG MF TITANIUN ALLOY BONE SCREW 1.0MM, 1.2MM, 1.3MM, 1.5MM, 1.7MM, 2.0MM, 2.4MM received FDA 510(k) clearance on 1998-03-13, under 510(k) number K974817.

Who is the listed applicant for DRG MF TITANIUN ALLOY BONE SCREW 1.0MM, 1.2MM, 1.3MM, 1.5MM, 1.7MM, 2.0MM, 2.4MM?

The FDA 510(k) record lists Doctor'S Research Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DRG MF TITANIUN ALLOY BONE SCREW 1.0MM, 1.2MM, 1.3MM, 1.5MM, 1.7MM, 2.0MM, 2.4MM?

The FDA product code for DRG MF TITANIUN ALLOY BONE SCREW 1.0MM, 1.2MM, 1.3MM, 1.5MM, 1.7MM, 2.0MM, 2.4MM is DZL.

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Other records listing Doctor'S Research Group, 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.

K051487DRG LARYNGEAL AUGMENTATION IMPLANT DEVICEK041018DRG SOFTRELEASEK012535DRG DISPOSABLE VAGINAL SPECULUMK012003DRG REACTION CHAMBER/SAFETY TIPK011736DRG QUICKMIXK013786DRG ORTHOHEX SS BONE SCREW

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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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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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