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FDA 510(k)

SYNTHES (USA) LOW-PROFILE WRIST FIXATOR

K-Number: K051049 · 2005-07-13

ApplicantSynthes (Usa)
Decision Date2005-07-13
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SYNTHES (USA) LOW-PROFILE WRIST FIXATOR is the device name listed in this FDA 510(k) record. The listed applicant is Synthes (Usa). It received FDA 510(k) clearance on 2005-07-13 under 510(k) number K051049. 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 SYNTHES (USA) LOW-PROFILE WRIST FIXATOR?

SYNTHES (USA) LOW-PROFILE WRIST FIXATOR is a medical device that received FDA 510(k) clearance on 2005-07-13. The listed applicant is Synthes (Usa). The 510(k) number is K051049.

When did SYNTHES (USA) LOW-PROFILE WRIST FIXATOR receive FDA 510(k) clearance?

SYNTHES (USA) LOW-PROFILE WRIST FIXATOR received FDA 510(k) clearance on 2005-07-13, under 510(k) number K051049.

Who is the listed applicant for SYNTHES (USA) LOW-PROFILE WRIST FIXATOR?

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 (USA) LOW-PROFILE WRIST FIXATOR?

The FDA product code for SYNTHES (USA) LOW-PROFILE WRIST FIXATOR is KTT.

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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: 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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