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FDA 510(k)

ARICULATED TENSION DEVICE SYNTHES TEN

K-Number: K792253 · 1979-12-05

ApplicantSynthes (Usa)
Decision Date1979-12-05
Product CodeHWN
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARICULATED TENSION DEVICE SYNTHES TEN is the device name listed in this FDA 510(k) record. The listed applicant is Synthes (Usa). It received FDA 510(k) clearance on 1979-12-05 under 510(k) number K792253. The device is classified under product code HWN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARICULATED TENSION DEVICE SYNTHES TEN?

ARICULATED TENSION DEVICE SYNTHES TEN is a medical device that received FDA 510(k) clearance on 1979-12-05. The listed applicant is Synthes (Usa). The 510(k) number is K792253.

When did ARICULATED TENSION DEVICE SYNTHES TEN receive FDA 510(k) clearance?

ARICULATED TENSION DEVICE SYNTHES TEN received FDA 510(k) clearance on 1979-12-05, under 510(k) number K792253.

Who is the listed applicant for ARICULATED TENSION DEVICE SYNTHES TEN?

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 ARICULATED TENSION DEVICE SYNTHES TEN?

The FDA product code for ARICULATED TENSION DEVICE SYNTHES TEN is HWN.

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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: HWN)

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.

K854241AOT EXTERNAL COMPRESS DEVICEAdvanced Ortho-Technology, Inc.K770349RIGID TEACHING ATTACHMENTRichard Wolf Medical Instruments Corp.K760970FLORIO CPC BANDRichard'S Medical Equip., Inc.

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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