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FDA 510(k)

EBI DFS JOINT FIXATOR, MODEL 02800

K-Number: K981483 · 1998-07-08

ApplicantElectro-Biology, Inc.
Decision Date1998-07-08
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EBI DFS JOINT FIXATOR, MODEL 02800 is the device name listed in this FDA 510(k) record. The listed applicant is Electro-Biology, Inc.. It received FDA 510(k) clearance on 1998-07-08 under 510(k) number K981483. 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 EBI DFS JOINT FIXATOR, MODEL 02800?

EBI DFS JOINT FIXATOR, MODEL 02800 is a medical device that received FDA 510(k) clearance on 1998-07-08. The listed applicant is Electro-Biology, Inc.. The 510(k) number is K981483.

When did EBI DFS JOINT FIXATOR, MODEL 02800 receive FDA 510(k) clearance?

EBI DFS JOINT FIXATOR, MODEL 02800 received FDA 510(k) clearance on 1998-07-08, under 510(k) number K981483.

Who is the listed applicant for EBI DFS JOINT FIXATOR, MODEL 02800?

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

What is the FDA product code for EBI DFS JOINT FIXATOR, MODEL 02800?

The FDA product code for EBI DFS JOINT FIXATOR, MODEL 02800 is KTT.

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Other records listing Electro-Biology, 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.

K992333EBI OMEGA 21 SYSTEMK992367EBI XFIX DYNAFIX SYSTEM HA COATED SCREWSK991941EBI XFIX DFS RAIL SYSTEMK990303EBI OMEGA 21 SYSTEMK991092EBI SPINELINK ANTERIOR CERVICAL SPINAL SYSTEMK990459EBI VUECATH ENDOSCOPIC SYSTEN

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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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