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FDA 510(k)

REPOSE BONE SCREW SYSTEM

K-Number: K981677 · 1999-08-27

ApplicantInfluence, Inc.
Decision Date1999-08-27
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

REPOSE BONE SCREW SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Influence, Inc.. It received FDA 510(k) clearance on 1999-08-27 under 510(k) number K981677. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPOSE BONE SCREW SYSTEM?

REPOSE BONE SCREW SYSTEM is a medical device that received FDA 510(k) clearance on 1999-08-27. The listed applicant is Influence, Inc.. The 510(k) number is K981677.

When did REPOSE BONE SCREW SYSTEM receive FDA 510(k) clearance?

REPOSE BONE SCREW SYSTEM received FDA 510(k) clearance on 1999-08-27, under 510(k) number K981677.

Who is the listed applicant for REPOSE BONE SCREW SYSTEM?

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

What is the FDA product code for REPOSE BONE SCREW SYSTEM?

The FDA product code for REPOSE BONE SCREW SYSTEM is LRK.

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Other records listing Influence, 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.

K991792CRYO-MONO CRYOGENIC SYSTEM, MODEL CRYO-MONO WITH TUF PROBEK992277STAPLETAC BONE ANCHOR SYSTEMK991122CRYO-MONO CRYOGRNIC SYSTEMK990160MICROTAC-BONE ANCHOR SYSTEMK990095STRAIGHT-IN-ORTHOPEDIC BONE SCREW FIXATION SYSTEMK983325IN-PROBE II URODYNAMIC SYSTEM

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Related Devices (Code: LRK)

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.

K262104Anti Snoring Mouthpiece (L09-BB, L09-PP, L09-TB, L09-BT, L09-TP, L09-PT, L09-TT)Ram.Shaw Pte., Ltd.K261912SnØreNegatØrDnB Innovations, LLCK261366VirtusSomnomed, Inc.K261251Snorbliss® Anti-Snoring DeviceEndeavor Commerce, LLCK261134Dormiva Anti-Snoring Mouth GuardKoncept Innovators, Inc.K252942ShaeferHShaeferh, LLC

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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