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FDA 510(k)

SL-PLUS AND SLR-PLUS

K-Number: K932481 · 1994-06-08

ApplicantEncore Orthopedics, Inc.
Decision Date1994-06-08
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SL-PLUS AND SLR-PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Encore Orthopedics, Inc.. It received FDA 510(k) clearance on 1994-06-08 under 510(k) number K932481. 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 SL-PLUS AND SLR-PLUS?

SL-PLUS AND SLR-PLUS is a medical device that received FDA 510(k) clearance on 1994-06-08. The listed applicant is Encore Orthopedics, Inc.. The 510(k) number is K932481.

When did SL-PLUS AND SLR-PLUS receive FDA 510(k) clearance?

SL-PLUS AND SLR-PLUS received FDA 510(k) clearance on 1994-06-08, under 510(k) number K932481.

Who is the listed applicant for SL-PLUS AND SLR-PLUS?

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

What is the FDA product code for SL-PLUS AND SLR-PLUS?

The FDA product code for SL-PLUS AND SLR-PLUS is JDI.

Other records listing Encore Orthopedics, Inc. as applicant

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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.

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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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