Atlas FDA

Surgical Navigation Advanced Platform (SNAP)

FDA 510(k) clearance K160584 · decided 2016-06-28

Clearance details

K-number
K160584
Device name
Surgical Navigation Advanced Platform (SNAP)
Applicant
Surgical Theater, LLC
Decision
Substantially Equivalent
Date received
2016-03-01
Decision date
2016-06-28
Days to decision
119 days
Clearance type
Traditional
Product code
LLZ
Device class
2
Regulation number
892.2050
Medical specialty
Radiology
Advisory committee
Radiology
Location
Mayfield Village, OH, US
Third-party review
No
Expedited review
No

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Recalls involving this device

RecordFirmDate
Surgical Navigation Advanced Platform (SNAP), software version SNP.3.12.0, imaging process recall (Z-0320-2026)Surgical Theater Inc2025-10-24
Surgical Navigation Advanced Platform Patient Engagement (PE SNAP), software version SNP.3 recall (Z-0321-2026)Surgical Theater Inc2025-10-24
SyncAR Surgical Navigation Advanced Platform Patient Engagement (SyncAR SNAP), software ve recall (Z-0322-2026)Surgical Theater Inc2025-10-24
Endo Surgical Navigation Advanced Platform Patient Engagement (EndoSNAP), software version recall (Z-0323-2026)Surgical Theater Inc2025-10-24