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FDA 510(k)

SYNTHES 7.0/7.3 MM CANNULATED SCREWS

K-Number: K962011 · 1996-08-05

ApplicantSynthes (Usa)
Decision Date1996-08-05
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

SYNTHES 7.0/7.3 MM CANNULATED SCREWS is the device name listed in this FDA 510(k) record. The listed applicant is Synthes (Usa). It received FDA 510(k) clearance on 1996-08-05 under 510(k) number K962011. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the SYNTHES 7.0/7.3 MM CANNULATED SCREWS?

SYNTHES 7.0/7.3 MM CANNULATED SCREWS is a medical device that received FDA 510(k) clearance on 1996-08-05. The listed applicant is Synthes (Usa). The 510(k) number is K962011.

When did SYNTHES 7.0/7.3 MM CANNULATED SCREWS receive FDA 510(k) clearance?

SYNTHES 7.0/7.3 MM CANNULATED SCREWS received FDA 510(k) clearance on 1996-08-05, under 510(k) number K962011.

Who is the listed applicant for SYNTHES 7.0/7.3 MM CANNULATED SCREWS?

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 7.0/7.3 MM CANNULATED SCREWS?

The FDA product code for SYNTHES 7.0/7.3 MM CANNULATED SCREWS is HWC. This falls under the Cardiovascular category.

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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: HWC)

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.

K262975Arthrex Beaming SystemArthrex, Inc.K260995DynaNail Helix® Fixation SystemMedShape, Inc.K254280F.A.S.T ScrewSteps OrthoK261057ActivaScrew™ Cannulated COMBioretec, Ltd.K260106OsteoCoil™ GT Active Compression SystemFlower Orthopedics Corporation DBA Conventus Flower OrthopedK262344Large Compression ScrewsTriMed, Inc.

Official Source

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

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