Pitkar Spinal Pedicle Screw System
K-Number: K240233 · 2024-09-09
Device Summary
Frequently Asked Questions
What is the Pitkar Spinal Pedicle Screw System?
Pitkar Spinal Pedicle Screw System is a medical device that received FDA 510(k) clearance on 2024-09-09. The listed applicant is S.H.Pitkar Orthotools Pvt. , Ltd.. The 510(k) number is K240233.
When did Pitkar Spinal Pedicle Screw System receive FDA 510(k) clearance?
Pitkar Spinal Pedicle Screw System received FDA 510(k) clearance on 2024-09-09, under 510(k) number K240233.
Who is the listed applicant for Pitkar Spinal Pedicle Screw System?
The FDA 510(k) record lists S.H.Pitkar Orthotools Pvt. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Pitkar Spinal Pedicle Screw System?
The FDA product code for Pitkar Spinal Pedicle Screw System is NKB.
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 S.H.Pitkar Orthotools Pvt. , Ltd. 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: NKB)
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.