SURGILASE YAG 100 IN ORTHOPEDIC SURGERY
K-Number: K900570 · 1990-05-01
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Device Summary
Frequently Asked Questions
What is the SURGILASE YAG 100 IN ORTHOPEDIC SURGERY?
SURGILASE YAG 100 IN ORTHOPEDIC SURGERY is a medical device that received FDA 510(k) clearance on 1990-05-01. The listed applicant is Surgilase, Inc.. The 510(k) number is K900570.
When did SURGILASE YAG 100 IN ORTHOPEDIC SURGERY receive FDA 510(k) clearance?
SURGILASE YAG 100 IN ORTHOPEDIC SURGERY received FDA 510(k) clearance on 1990-05-01, under 510(k) number K900570.
Who is the listed applicant for SURGILASE YAG 100 IN ORTHOPEDIC SURGERY?
The FDA 510(k) record lists Surgilase, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SURGILASE YAG 100 IN ORTHOPEDIC SURGERY?
The FDA product code for SURGILASE YAG 100 IN ORTHOPEDIC SURGERY is GEX. This falls under the Gastroenterology category.
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 Surgilase, 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.
Related Devices (Code: GEX)
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
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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