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FDA 510(k)

STALIF (TM) C

K-Number: K072415 · 2008-01-25

ApplicantSurgicraft , Ltd.
Decision Date2008-01-25
Product CodeOVE
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

STALIF (TM) C is the device name listed in this FDA 510(k) record. The listed applicant is Surgicraft , Ltd.. It received FDA 510(k) clearance on 2008-01-25 under 510(k) number K072415. The device is classified under product code OVE. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STALIF (TM) C?

STALIF (TM) C is a medical device that received FDA 510(k) clearance on 2008-01-25. The listed applicant is Surgicraft , Ltd.. The 510(k) number is K072415.

When did STALIF (TM) C receive FDA 510(k) clearance?

STALIF (TM) C received FDA 510(k) clearance on 2008-01-25, under 510(k) number K072415.

Who is the listed applicant for STALIF (TM) C?

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

What is the FDA product code for STALIF (TM) C?

The FDA product code for STALIF (TM) C is OVE.

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Other records listing Surgicraft , 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.

K091207SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (AC) DEVICEK072370SURGICRAFT SURGICAL MESH SYSTEMK080447SURGICRAFT SCREW FIXATION SYSTEMK073109STALIF TT INTERVERTEBRAL BODY FUSION SYSTEMK051027STALIF TTK041617STALIF TT

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Related Devices (Code: OVE)

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.

K263049SABER-C SystemElevation SpineK261882Pisces-SC Standalone Cervical Interbody SystemOsseus Fusions Systems, LLCK261451ZSAlign Cervical Interbody SystemZSFab, Inc.K262094E3D™-C Interbody SystemEvolution SpineK261279DeltaNEC Interbody SystemNexus SpineK252982CONDUIT™ ZERO-P™ VA Secured Spacer SystemAvalign Technologies, Inc.

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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