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FDA 510(k)

P.M.D. INTRAMEDULLARY CEMENT RESTRICTOR PLUG

K-Number: K863854 · 1986-11-19

ApplicantPrecision Medical Devices, Inc.
Decision Date1986-11-19
Product Code
DecisionSubstantially Equivalent

Device Summary

P.M.D. INTRAMEDULLARY CEMENT RESTRICTOR PLUG is the device name listed in this FDA 510(k) record. The listed applicant is Precision Medical Devices, Inc.. It received FDA 510(k) clearance on 1986-11-19 under 510(k) number K863854. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P.M.D. INTRAMEDULLARY CEMENT RESTRICTOR PLUG?

P.M.D. INTRAMEDULLARY CEMENT RESTRICTOR PLUG is a medical device that received FDA 510(k) clearance on 1986-11-19. The listed applicant is Precision Medical Devices, Inc.. The 510(k) number is K863854.

When did P.M.D. INTRAMEDULLARY CEMENT RESTRICTOR PLUG receive FDA 510(k) clearance?

P.M.D. INTRAMEDULLARY CEMENT RESTRICTOR PLUG received FDA 510(k) clearance on 1986-11-19, under 510(k) number K863854.

Who is the listed applicant for P.M.D. INTRAMEDULLARY CEMENT RESTRICTOR PLUG?

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

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.

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Other records listing Precision Medical Devices, 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.

K840856MODULAR CONSTRUCT FRAME EXTERNAL FIXAK840046PRESSURIZING/SCAVENGING ACRYLIC CEMENT

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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