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FDA 510(k)

NATURAL HIP SYSTEM POROUS STEM - COLLARLESS, COLLARED

K-Number: K963266 · 1996-10-15

Decision Date1996-10-15
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NATURAL HIP SYSTEM POROUS STEM - COLLARLESS, COLLARED is the device name listed in this FDA 510(k) record. The listed applicant is Intermedics Orthopedics. It received FDA 510(k) clearance on 1996-10-15 under 510(k) number K963266. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NATURAL HIP SYSTEM POROUS STEM - COLLARLESS, COLLARED?

NATURAL HIP SYSTEM POROUS STEM - COLLARLESS, COLLARED is a medical device that received FDA 510(k) clearance on 1996-10-15. The listed applicant is Intermedics Orthopedics. The 510(k) number is K963266.

When did NATURAL HIP SYSTEM POROUS STEM - COLLARLESS, COLLARED receive FDA 510(k) clearance?

NATURAL HIP SYSTEM POROUS STEM - COLLARLESS, COLLARED received FDA 510(k) clearance on 1996-10-15, under 510(k) number K963266.

Who is the listed applicant for NATURAL HIP SYSTEM POROUS STEM - COLLARLESS, COLLARED?

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

What is the FDA product code for NATURAL HIP SYSTEM POROUS STEM - COLLARLESS, COLLARED?

The FDA product code for NATURAL HIP SYSTEM POROUS STEM - COLLARLESS, COLLARED is LPH.

Related Clinical Trials

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.

Other records listing Intermedics Orthopedics 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.

View all 108 devices →

Related Devices (Code: LPH)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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