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FDA 510(k)

ALPHATEC 130-150 SLOTTED COMPRESSION HIP SCREW

K-Number: K926417 · 1994-09-28

ApplicantAlphatec Mfg., Inc.
Decision Date1994-09-28
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ALPHATEC 130-150 SLOTTED COMPRESSION HIP SCREW is the device name listed in this FDA 510(k) record. The listed applicant is Alphatec Mfg., Inc.. It received FDA 510(k) clearance on 1994-09-28 under 510(k) number K926417. 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 ALPHATEC 130-150 SLOTTED COMPRESSION HIP SCREW?

ALPHATEC 130-150 SLOTTED COMPRESSION HIP SCREW is a medical device that received FDA 510(k) clearance on 1994-09-28. The listed applicant is Alphatec Mfg., Inc.. The 510(k) number is K926417.

When did ALPHATEC 130-150 SLOTTED COMPRESSION HIP SCREW receive FDA 510(k) clearance?

ALPHATEC 130-150 SLOTTED COMPRESSION HIP SCREW received FDA 510(k) clearance on 1994-09-28, under 510(k) number K926417.

Who is the listed applicant for ALPHATEC 130-150 SLOTTED COMPRESSION HIP SCREW?

The FDA 510(k) record lists Alphatec Mfg., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALPHATEC 130-150 SLOTTED COMPRESSION HIP SCREW?

The FDA product code for ALPHATEC 130-150 SLOTTED COMPRESSION HIP SCREW is KTT.

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Other records listing Alphatec Mfg., Inc. 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.

K033090ICON POLYAXIAL PEDICLE SCREW SYSTEMK023299ALPHA MIRAGE TOP TIGHTENING SPINAL SYSTEMK020356ALPHA MIRAGE TOP TIGHTENING SPINAL SYSTEMK993513DELTALOC ANTERIOR CERVICAL PLATE SYSTEMK993873ALPHATEC EXTERNAL FIXATION SYSTEM COMPRESSION/DISTRACTION RODK992350PYLON INTRAMEDULLAARY NAIL SYSTEM

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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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