FDA 510(k)

VSP HIP STEM

K-Number: K903957 · 1990-11-26

Decision Date1990-11-26

Product CodeJDI

Advisory CommitteeOR

DecisionSubstantially Equivalent for Some Indications

Device Summary

VSP HIP STEM is the device name listed in this FDA 510(k) record. The listed applicant is Turnkey Intergration USA, Inc.. It received FDA 510(k) clearance on 1990-11-26 under 510(k) number K903957. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the VSP HIP STEM?

VSP HIP STEM is a medical device that received FDA 510(k) clearance on 1990-11-26. The listed applicant is Turnkey Intergration USA, Inc.. The 510(k) number is K903957.

When did VSP HIP STEM receive FDA 510(k) clearance?

VSP HIP STEM received FDA 510(k) clearance on 1990-11-26, under 510(k) number K903957.

Who is the listed applicant for VSP HIP STEM?

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

What is the FDA product code for VSP HIP STEM?

The FDA product code for VSP HIP STEM is JDI.

Other records listing Turnkey Intergration USA, 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.

K991405OMNI-FIX, HUMERAL NAIL K990523B2C, ESPACE REVISION CUP SYSTEM K990307OMNI-FIX, NAIL SYSTEM K972411LINK CEMENT PLUG K970284ARTOS, DIPLOS SYSTEM K970084LINK CERCLAGE WIRE SYSTEM

View all 26 devices →

Related Devices (Code: JDI)

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 Biomet K240783Anthology 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 Orthopaedics K240418Stryker 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.