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FDA 510(k)

VHS PEDIATRIC HIP SCREW SYSTEM

K-Number: K011603 · 2001-08-15

ApplicantWalter Abendschein, M.D.
Decision Date2001-08-15
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VHS PEDIATRIC HIP SCREW SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Walter Abendschein, M.D.. It received FDA 510(k) clearance on 2001-08-15 under 510(k) number K011603. 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 VHS PEDIATRIC HIP SCREW SYSTEM?

VHS PEDIATRIC HIP SCREW SYSTEM is a medical device that received FDA 510(k) clearance on 2001-08-15. The listed applicant is Walter Abendschein, M.D.. The 510(k) number is K011603.

When did VHS PEDIATRIC HIP SCREW SYSTEM receive FDA 510(k) clearance?

VHS PEDIATRIC HIP SCREW SYSTEM received FDA 510(k) clearance on 2001-08-15, under 510(k) number K011603.

Who is the listed applicant for VHS PEDIATRIC HIP SCREW SYSTEM?

The FDA 510(k) record lists Walter Abendschein, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VHS PEDIATRIC HIP SCREW SYSTEM?

The FDA product code for VHS PEDIATRIC HIP SCREW SYSTEM is KTT.

Related Clinical Trials

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.

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Other records listing Walter Abendschein, M.D. 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.

K002184COD COMPRESSION OSTEOTOMY DEVICEK000827UNICOMPARTMENTAL PATELLOFEMORAL PROSTHESIS (UPP) CEMENTEDK991806VHS SUPRACONDYLAR PLATE SYSTEMK964880VARI-ANGLE HIP SCREW (VHS) SYSTEM

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

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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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