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FDA 510(k)

SYNTHES LIMITED CONTACT-DYNAMIC HIP SCREW IMPLANT

K-Number: K923613 · 1993-06-22

ApplicantSynthes (Usa)
Decision Date1993-06-22
Product CodeJDO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SYNTHES LIMITED CONTACT-DYNAMIC HIP SCREW IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Synthes (Usa). It received FDA 510(k) clearance on 1993-06-22 under 510(k) number K923613. The device is classified under product code JDO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNTHES LIMITED CONTACT-DYNAMIC HIP SCREW IMPLANT?

SYNTHES LIMITED CONTACT-DYNAMIC HIP SCREW IMPLANT is a medical device that received FDA 510(k) clearance on 1993-06-22. The listed applicant is Synthes (Usa). The 510(k) number is K923613.

When did SYNTHES LIMITED CONTACT-DYNAMIC HIP SCREW IMPLANT receive FDA 510(k) clearance?

SYNTHES LIMITED CONTACT-DYNAMIC HIP SCREW IMPLANT received FDA 510(k) clearance on 1993-06-22, under 510(k) number K923613.

Who is the listed applicant for SYNTHES LIMITED CONTACT-DYNAMIC HIP SCREW IMPLANT?

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

What is the FDA product code for SYNTHES LIMITED CONTACT-DYNAMIC HIP SCREW IMPLANT?

The FDA product code for SYNTHES LIMITED CONTACT-DYNAMIC HIP SCREW IMPLANT is JDO.

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Other records listing Synthes (Usa) 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.

K121601SYNTHES 2.7/3.5MM VARIABLE ANGLE LCP ANKLE TRAUMA SYSTEM-ANTEROLATERAL DISTAL TIBIA PLATEK120854SYNTHES VA LCP ANKLE TRAUMA SYSTEMK120717SYNTHES VARIABLE ANGLE LCP ELBOW SYSTEM (MEDICAL AND POSTEROLATERAL DISTAL HUMERUS PLATES)K120070SYNTHES VARIABLE ANGLE LCP ELBOW SYSTEMK120083SET SCREW FOR TI TROCHANTERIC FIXATION NAIL(TFN)K111667SYNTHES SUPRAPATELLAR INSERTION INSTRUMENTS

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Related Devices (Code: JDO)

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.

K230764OsteoCentric Integrated Hip Fastener SystemOsteoCentric TechnologiesK213126Smith & Nephew, Inc. Plates and Screws Systems: EVOS, Peri-Loc, D-Rad, TC-100, VLP Mini-Mod, Compression Hip Screw (CHS), CONQUEST FN, and cannulated screwsSmith & Nephew, Inc.K210247OsteoCentric Integrated Hip Fastener SystemOsteocentric Technologies D.B.A. Osteocentric TraumaK193029CONQUEST FNSmith & Nephew, Inc.K173826THP Hip Fracture Plating SystemBiomet, Inc.K172785CONQUEST FNSmith & Nephew

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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