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FDA 510(k)

AUTODYNAMIC COMPRESSION HIP SCREW-PLATE

K-Number: K843449 · 1984-10-22

ApplicantMecron Medical Products, Inc.
Decision Date1984-10-22
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AUTODYNAMIC COMPRESSION HIP SCREW-PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Mecron Medical Products, Inc.. It received FDA 510(k) clearance on 1984-10-22 under 510(k) number K843449. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTODYNAMIC COMPRESSION HIP SCREW-PLATE?

AUTODYNAMIC COMPRESSION HIP SCREW-PLATE is a medical device that received FDA 510(k) clearance on 1984-10-22. The listed applicant is Mecron Medical Products, Inc.. The 510(k) number is K843449.

When did AUTODYNAMIC COMPRESSION HIP SCREW-PLATE receive FDA 510(k) clearance?

AUTODYNAMIC COMPRESSION HIP SCREW-PLATE received FDA 510(k) clearance on 1984-10-22, under 510(k) number K843449.

Who is the listed applicant for AUTODYNAMIC COMPRESSION HIP SCREW-PLATE?

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

What is the FDA product code for AUTODYNAMIC COMPRESSION HIP SCREW-PLATE?

The FDA product code for AUTODYNAMIC COMPRESSION HIP SCREW-PLATE is KTT.

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Other records listing Mecron Medical Products, 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.

K861138MASH DERMATOMEK854191MECRON UNCEMENTED STRUCTURED STEM HIPK844775EFFNER-EYE CAUTERY WITH BATTERY HANDLEK844774EFFNER FIBER OPTIC CABLES FOR COLD LIGHT TRANSMISSK844488MECRON CEMENTED STRUCTURED STEM HIP PROSTHESISK844486MECRON MRC-HEADLESS FEMORAL COMPONENT

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Related Devices (Code: KTT)

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.

K254087MAXFRAME AUTOSTRUT™ with Bluetooth Multi-Axial Correction SystemSynthes (USA) Products, LLCK260900DYNEX® External Fixation SystemsVilex, LLCK260112QuikFix External Fixator: Knee-Spanning PackStabiliz Orthopaedics, Inc.K253291Excelsior SystemBlue Ocean GlobalK253613Monkey Rings External Ring Fixation SystemParagon 28, Inc.K253202Hoffmann LRF SystemStryker 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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