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FDA 510(k)

HOFFMANN LRF (LIMB RECONSTRUCTION FRAME SYSTEM)

K-Number: K130334 · 2013-05-03

ApplicantStryker Trauma AG
Decision Date2013-05-03
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HOFFMANN LRF (LIMB RECONSTRUCTION FRAME SYSTEM) is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Trauma AG. It received FDA 510(k) clearance on 2013-05-03 under 510(k) number K130334. 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 HOFFMANN LRF (LIMB RECONSTRUCTION FRAME SYSTEM)?

HOFFMANN LRF (LIMB RECONSTRUCTION FRAME SYSTEM) is a medical device that received FDA 510(k) clearance on 2013-05-03. The listed applicant is Stryker Trauma AG. The 510(k) number is K130334.

When did HOFFMANN LRF (LIMB RECONSTRUCTION FRAME SYSTEM) receive FDA 510(k) clearance?

HOFFMANN LRF (LIMB RECONSTRUCTION FRAME SYSTEM) received FDA 510(k) clearance on 2013-05-03, under 510(k) number K130334.

Who is the listed applicant for HOFFMANN LRF (LIMB RECONSTRUCTION FRAME SYSTEM)?

The FDA 510(k) record lists Stryker Trauma AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HOFFMANN LRF (LIMB RECONSTRUCTION FRAME SYSTEM)?

The FDA product code for HOFFMANN LRF (LIMB RECONSTRUCTION FRAME SYSTEM) is KTT.

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Other records listing Stryker Trauma AG 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.

K172210ReUnion Reversible Fracture System (RFX), ReUnion Reverse Shoulder Arthroplasty System (RSA), ReUnion Total Shoulder Arthroplasty System (TSA)K133440AXSOS 3 TI LOCKING PLATE SYSTEM LINE EXTENSIONK132502VARIAX 2 SYSTEMK131365T2 TIBIAL NAILING SYSTEMK130907HOFFMANN LRF (LIMB RECONSTRUCTION FRAME) SYSTEMK131132PELVIS II IMPLANT 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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