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FDA 510(k)

DRG TITANIUM BONE PLATE

K-Number: K990920 · 1999-06-10

ApplicantDoctor'S Research Group, Inc.
Decision Date1999-06-10
Product CodeJEY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DRG TITANIUM BONE PLATE 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 1999-06-10 under 510(k) number K990920. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRG TITANIUM BONE PLATE?

DRG TITANIUM BONE PLATE is a medical device that received FDA 510(k) clearance on 1999-06-10. The listed applicant is Doctor'S Research Group, Inc.. The 510(k) number is K990920.

When did DRG TITANIUM BONE PLATE receive FDA 510(k) clearance?

DRG TITANIUM BONE PLATE received FDA 510(k) clearance on 1999-06-10, under 510(k) number K990920.

Who is the listed applicant for DRG TITANIUM BONE PLATE?

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 TITANIUM BONE PLATE?

The FDA product code for DRG TITANIUM BONE PLATE is JEY.

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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 Devices (Code: JEY)

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.

K260137KLS Martin IPS Oral-Max Implants - MR Conditional; Individual Patient Solutions - Ti (IPS-Ti); Individual Patient Solutions - PEEK (IPS-PEEK); KLS Martin Individual Patient SolutionsKLS-Martin L.P.K253206METICULY Patient-specific CMF solutionMeticuly Co., Ltd.K252246Leforte MMF SystemJeil Medical CorporationK253373Southern Craniomaxillofacial (CMF) SystemSouthern Medical (Pty) , Ltd.K251441Inion CPS 1.5 Baby Bioabsorbable Fixation System; Inion CPS 1.5/2.0/2.5 Bioabsorbable Fixation SystemInion OYK241314KLS Martin Oral-Max Implants MR Conditional (bundled)KLS-Martin L.P.

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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