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FDA 510(k)

POLYMER THREADED ANCHOR / SUTURE COMBINATION

K-Number: K982963 · 1998-11-20

ApplicantOrthopaedic Biosystems, Ltd.
Decision Date1998-11-20
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

POLYMER THREADED ANCHOR / SUTURE COMBINATION is the device name listed in this FDA 510(k) record. The listed applicant is Orthopaedic Biosystems, Ltd.. It received FDA 510(k) clearance on 1998-11-20 under 510(k) number K982963. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POLYMER THREADED ANCHOR / SUTURE COMBINATION?

POLYMER THREADED ANCHOR / SUTURE COMBINATION is a medical device that received FDA 510(k) clearance on 1998-11-20. The listed applicant is Orthopaedic Biosystems, Ltd.. The 510(k) number is K982963.

When did POLYMER THREADED ANCHOR / SUTURE COMBINATION receive FDA 510(k) clearance?

POLYMER THREADED ANCHOR / SUTURE COMBINATION received FDA 510(k) clearance on 1998-11-20, under 510(k) number K982963.

Who is the listed applicant for POLYMER THREADED ANCHOR / SUTURE COMBINATION?

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

What is the FDA product code for POLYMER THREADED ANCHOR / SUTURE COMBINATION?

The FDA product code for POLYMER THREADED ANCHOR / SUTURE COMBINATION is JDI.

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Other records listing Orthopaedic Biosystems, Ltd. 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.

K000797OBL 2.0 MM MINI TAC ANCHOR, MODEL 10-1629-01K982996POLYMER OBL SB ANCHOR / SUTURE COMBINATIONK983169POLYMER THREADED ANCHORK972326PEBA ANCHOR/SUTURE COMBINATIONK963420CANCELLOUS SCREW WASHERK963432GUIDE WIRES FOR CANNULATED SCREWS

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Related Devices (Code: JDI)

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.

K253515Zimmer Biomet OSS™ Orthopedic Salvage System OsseoTi® Sleeves and AugmentsBiomet Orthopedics, Inc.K253434OSSTM Orthopedic Salvage SystemBiomet, Inc.K243571Trabecular Metal Acetabular Revision System, Acetabular Liners and Constrained LinersZimmer BiometK240783Anthology Hip Stems; CPCS Hip Stems; Femoral Heads; R3 Acetabular Liners; Spectron Hip Stems; Synergy Hip StemsSmith & Nephew, Inc.K241716Global Modular Replacement System, Modular Replacement System, Modular Rotating Hinge Knee ComponentHowmedica Osteonics Corp., Dba Stryker OrthopaedicsK240418Stryker Orthopaedics Hip Systems Labeling UpdateHowmedica Osteonics Corp., Dba Stryker Orthopaedics

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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