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FDA 510(k)

FEMORAL INTRAMEDULLARY RODS

K-Number: K926465 · 1993-08-25

ApplicantApplied Osteo Systems, Inc.
Decision Date1993-08-25
Product CodeJDS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FEMORAL INTRAMEDULLARY RODS is the device name listed in this FDA 510(k) record. The listed applicant is Applied Osteo Systems, Inc.. It received FDA 510(k) clearance on 1993-08-25 under 510(k) number K926465. The device is classified under product code JDS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FEMORAL INTRAMEDULLARY RODS?

FEMORAL INTRAMEDULLARY RODS is a medical device that received FDA 510(k) clearance on 1993-08-25. The listed applicant is Applied Osteo Systems, Inc.. The 510(k) number is K926465.

When did FEMORAL INTRAMEDULLARY RODS receive FDA 510(k) clearance?

FEMORAL INTRAMEDULLARY RODS received FDA 510(k) clearance on 1993-08-25, under 510(k) number K926465.

Who is the listed applicant for FEMORAL INTRAMEDULLARY RODS?

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

What is the FDA product code for FEMORAL INTRAMEDULLARY RODS?

The FDA product code for FEMORAL INTRAMEDULLARY RODS is JDS.

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Other records listing Applied Osteo Systems, 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.

K935383FEMROD AND FEMROD RECON INSERTK933995TRUE/FLEXTM FEMUR RODS, CAPS, SCREWS AND INSTRUMENTATIONK944501TRUE/FLEX INTRAMEDULLARY ROD END-CAPK941048TRUE/LOK MONOLATERAL/BILATERAL FIXATORK943160INTERFERENCE SCREWK934148TRUE/FLEX CLAVICLE RODS

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Related Devices (Code: JDS)

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.

K243608TRIGEN Stable Lock Nut & WasherSmith & Nephew, Inc.K240061TRIGEN MAX Tibial Nail System; INTERTAN MAX Hip Fracture Nail SystemSmith & Nephew, Inc.K241804TRIGEN INTERTAN 10S Nail SystemSmith & Nephew, Inc.K233150NET BRAND Osteosynthesis Nailing SystemNarang Medical , Ltd.K230761TRIGEN META-NAIL Nail SystemSmith & Nephew, Inc.K201336DePuy Synthes Tibial Nail Advanced, Depuy Synthes Locking Screws Medullary Nails, 4.0 and 5.0mmSynthes (USA) Products, 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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